Acenocoumarol versus Nadroparin | |||
Hamulyak, 1994 | Acenocoumarol versus Nadroparin 60 anti-Xa IU /kg x1 | THR or TKR (stratified) | single blind Follow-up duration: Day 10 ± 2 |
Acenocoumarol versus Reviparin | |||
Samama, 2001 | Acenocoumarol versus Reviparin 4200 anti-Xa IU x1 | THR | Open Follow-up duration: 6 weeks |
Acenocoumarol versus unfractionated heparin | |||
van Geloven, 1977 | Acenocoumarol versus UFH 4000 ·x2 | THR | double blind Follow-up duration: NA |
antixarin versus unfractionated heparin | |||
Limmer, 1994 | Antixarin 2500 anti Xa units versus UFH 15 000 units | General surgery | Open |
apixaban versus enoxaparin | |||
ADVANCE 3, 2010 NCT00423319 | apixaban 2.5mg twice daily for 35 days versus enoxaparin 40mg once daily for 35 days | patients undergoing elective total hip replacement surgery | double blind Follow-up duration: 35 days (+60) 21 countries |
ADOPT, 2011 NCT00457002 | apixaban, administered orally at a dose of 2.5 mg twice daily for 30 days versus enoxaparin, administered subcutaneously at a dose of 40 mg once daily for 6 to 14 days | acutely ill patients who had congestive heart failure or respiratory failure or other medical disorders and at least one additional risk factor for venous thromboembolism and who were hospitalized with an expected stay of at least 3 days | double-blind Follow-up duration: 30 days |
apixaban versus enoxaparin (europe regimen) | |||
ADVANCE 2, 2010 NCT00452530 | apixaban 2.5mg twice daily during 12 days versus enoxaparin 40mg once daily 12 days | patients undergoing elective unilateral or bilateral total knee replacement | double blind Follow-up duration: 12 days 27 countries |
apixaban versus enoxaparin (US regimen) | |||
APROPOS 2.5mg, 2007 NCT00097357 | apixaban 2.5mg BID for 12 days versus enoxaparin 30mg twice daily for 12 days | patients undergoing elective total knee replacement surgery | double blind Follow-up duration: 12 days |
ADVANCE-1, 2008 NCT00371683 | apixaban 2.5 mg orally twice daily for 10 to 14 days versus enoxaparin 30mg subcutaneously every 12 hours for 10-14 days | patients undergoing knee-replacement surgery | double blind Follow-up duration: 10-14 days 14 countries |
ardeparin versus placebo | |||
Levine, 1996 | ardeparin 50/kgx2 +elastic stockings versus Placebo+elastic stockings | Knee | double blind Follow-up duration: 14 days |
ardeparin versus unfractionated heparin | |||
Godwin, 1993 | Ardeparin 90 and 50 units/kg b.i.d versus UFH 10 000 units | Abdominopelvic surgery | Blind |
aspirin versus control | |||
Clagett, 1975 | A1300 versus control | open | |
Zekert VI, 1982 | A1500 versus control | open | |
Aspirin versus no treatment | |||
Pasteyer, 1977 | Aspirin 1000mg daily + Hep versus control (Hep alone) | Elective orthopaedic surgery | Follow-up duration: 2 weeks |
Rocha, 1986 | Aspirin 250mg or 1000mg daily versus control (combination of heparin plus dihydroergotamine) | total hip replacement | open Follow-up duration: 1 weeks |
aspirin versus placebo | |||
MRC, 1972 | A600 versus placebo | general surgery | double-blind |
Loew DVT, 1974 | A600 versus Placebo | double-blind | |
Erfurt-A, 1979 | A1500 versus Placebo | double-blind | |
Zekert V, 1980 | A1500+Hep??? versus Placebo | double-blind | |
Vinazzer I, 1980 | A1500+Hep v Hep versus Placebo | double-blind | |
Vinazzer II, 1977 | A1000+Hepv Hep versus Placebo | double-blind | |
Aspirin versus placebo | |||
Zekert-I , 1974 | Aspirin 1500mg daily versus placebo | patients undergoing surgery of hip-joint proximal fractures | double-blind |
Powers , 1976 | A1300 versus placebo | traumatic orthopaedic surgery | |
Erfurt-B , 1979 | A1500 versus placebo | traumatic orthopaedic surgery | double-blind |
aspirin versus placebo | |||
PEP hip-fracture, 2000 | aspirin 160mg/d started preoperatively and continued for 35 days versus placebo | patients undergoing surgery for hip fracture | Double blind Follow-up duration: 35 days Australia, New Zealand, South Africa, |
PEP elective arthroplasty, 2000 | aspirin 160mg/d started preoperatively and continued for 35 daysA versus placebo | Patients undergoing elective hip or knee arthroplasty | Double blind Follow-up duration: 35 days New Zealand |
Aspirin versus placebo | |||
Stockholm-I, 1975 | Aspirin 2000mg daily versus placebo | elective surgery of the hip | double blind Follow-up duration: 2 weeks |
Harris-I, 1977 | Aspirin 1200mg daily versus placebo | patients over 40 years of age, who had undergone total hip replacement | double-blind Follow-up duration: 1 weeks |
McKenna-I, 1980 | Aspirin 975mg or 3900mg daily versus placebo | total knee replacement | double-blind Follow-up duration: 2 weeks |
Sautter, 1983 | Aspirin 900mg daily + sulfinpyrazone versus placebo | patient with total hip replacement | Follow-up duration: 3 weeks |
McBride, 1983 | A1800+Dipyridamole versus placebo | Elective orthopaedic surgery | Follow-up duration: 1 weeks |
aspirin + dipyridamol versus control | |||
Chicago, 1982 | aspirin, 300 mg bid, and dipyridamole, 75 mg tid versus control | patients with acute spinal cord injury | open |
aspirin + dipyridamol versus no treatment | |||
Morris-B , 1977 | Aspirin 900 mg daily + dipyridamole versus control | elderly patients with hip fractures | open |
Lyon-I, 1975 | Aspirin 1500 mg daily + Dipyridamole versus control | Elective orthopaedic surgery | Follow-up duration: 2 weeks |
aspirin + dipyridamol versus placebo | |||
Encke-II , 1976 | Aspirin 1500mg daily, Aspirin 990mg daily + dipyridamol versus placebo | patients with abdominal operations | double-blind |
Hamburg, 1976 | A+Dipyridamole,A1000 versus placebo | Elective orthopaedic surgery | Follow-up duration: 3 weeks |
Frankfurt, 1981 | A+Dip,A1320 versus placebo | patients with myocardial infarction | double-blind |
betrixaban versus enoxaparin | |||
APEX, 2016 NCT01583218 | betrixaban (at a dose of 80 mg once daily) for 35 to 42 days versus subcutaneous enoxaparin (at a dose of 40 mg once daily) for 10±4 days | Patients who were hospitalized for acute medical illnesses and with an elevated d-dimer level | double-blind |
CECT versus IPC | |||
Murakami, 2003 | miniaturized sequential device continuous enhanced-circulation therapy CECT versus standard calf-length sequential IPC device | Adult trauma patients recruited in emergency department | open United States |
CECT + aspirin versus LMWH | |||
Gelfer, 2006 | continuous enhanced circulation therapy (CECT) combined with low-dose aspirin versus enoxaparin 40 mg daily | patients who underwent total hip or knee arthroplasty | open Follow-up duration: 8 days |
certoparin versus control | |||
Kock, 1995 | Certoparin 3000 IU versus no prophylaxis | patients with minor injuries treated with plaster-cast immobilisation of the leg | open Follow-up duration: 15 days |
certoparin versus UFH | |||
CERTIFY, 2010 | versus | ||
certoparin versus unfractionated heparin | |||
Schmitz-Huebner, 1984 | Certoparin (dose 1 and dose 2) b.i.d. versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 1 month |
Sasahara, 1986 | Certoparin 3000 + DHE versus UFH 10 000 units +DHE | Abdominal surgery | Blind Follow-up duration: 7 days |
Voigt, 1986 | Certoparin 3000 + DHE versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 10 days |
Welzel, 1988 | Certoparin 2500 + DHE versus UFH 10 000 units+DHE | Abdominal surgery | Open Follow-up duration: 7 days |
Kakkar, 1989 | Certoparin 3000 + DHE versus UFH 10 000 units+DHE | Abdominal surgery | Blind |
Adolf, 1989 | Certoparin 3000 versus UFH 15 000 units | Abdominal surgery | Blind Follow-up duration: 1 month |
Heilmann, 1989 | Certoparin 3000 versus UFH 15 000 units | Gynaecological surgery | Blind Follow-up duration: 10 days |
Baumgartner, 1989 | Certoparin 3000 + DHE versus UFH 5 000 units+DHE | Abdominal surgery | Blind Follow-up duration: 10 days |
Hoffmann and Largiade, 1990 | Certoparin 3000 + DHE versus UFH 10 000 units | Abdominal surgery | NA |
Koppenhagen, 1990 | Certoparin 3000 anti Xa units versus UFH 15 000 units | Abdominal surgery | Blind |
Schielke, 1991 | Certoparin 3000 anti Xa units + DHE versus UFH 10 000 units + DHE | Abdominal surgery | Open |
Koppenhagen, 1992 | Certoparin 3000 anti Xa units versus UFH 15 000 units | Abdominal surgery | Blind |
Hoffmann and Largiader, 1992 | Certoparin 3000 anti Xa units versus UFH 10 000 units | Abdominothoracic surgery | Blind |
Heilmann, 1997 | Certoparin 3000 anti Xa units versus UFH 15 000 units | Gynaecological and breast surgery | Blind |
Haas, 1999 | Certoparin 3000 anti Xa units versus UFH 15 000 units | General surgery | Blind |
certoparine + DHE versus Unfractionated heparin | |||
Haas , 1987 | Sandoz +0.5mg DHE versus Unfractionated heparin | Elective hip | |
Lassen, 1989 | certoparin 3000+0.5mg DHE x1 versus placebo | Hip fracture | double blind Follow-up duration: 6 days |
Lassen, 1988 | certoparin 3000+0.5mg DHE, x1 versus Placebo | Elective hip | double blind Follow-up duration: 6 days |
compression stocking group versus control (on top fondaparinux) | |||
Cohen (L8405), 2007 | fondaparinux 2.5mg plus graduated compression stockings versus fondaparinux 2.5mg daily | patients undergoing elective or emergency hip surgery | open Follow-up duration: 42 days Brazil, UK, Hong Kong, Spain |
dabigatran 150mg versus enoxaparin | |||
RE-NOVATE (150mg), 2007 NCT00168818 | dabigatran etexilate 150 mg q.d. 28-35 days
versus Enoxaparin 40 mg q.d. for 28-25 days | Total hip replacement | double blind Follow-up duration: 28-35 days, median 33d Europe, Australia, South Africa |
dabigatran 150mg versus enoxaparin (europe regimen) | |||
RE-MODEL (150mg), 2007 | dabigatran etexilate 150 mg q.d. for 6-10 days versus Enoxaparin 40 mg q.d. for 6-10 days | Total knee replacement | double blind Follow-up duration: 6-10 days, mean 8 days Europe, Australia, South Africa |
dabigatran 150mg versus enoxaparin (US regimen) | |||
RE-MOBILIZE (150mg), 2008 | dabigatran etexilate 150 mg q.d. for 12-15 days
versus enoxaparin 30 mg SC BID after surgery for 12-15 days | Total knee replacement | double blind Follow-up duration: 12-15 days, median 14d US, Canada, Mexico, UK |
dabigatran 220mg versus enoxaparin | |||
RE-NOVATE 2, 0 NCT00657150 | dabigatran 220mg once daily for 28-35 Days versus enoxaparin 40mg subcutaneous once daily for 28-35 Days | patients undergoing total hip-replacement surgery | double-blind Follow-up duration: 28-35 days (mean 32d) |
RE-NOVATE (220mg), 2007 NCT00168818 | dabigatran etexilate 220 mg q.d. for 28-35 days versus Enoxaparin 40 mg q.d. for 23-35 days | Total hip replacement | double blind Follow-up duration: 28-35 days, median 33d Europe, Australia, South Africa |
dabigatran 220mg versus enoxaparin (europe regimen) | |||
RE-MODEL (220mg), 2007 | dabigatran etexilate 220 mg q.d. 6-10 days
versus Enoxaparin 40 mg q.d. for 6-10 days | patients undergoing total knee replacement | double blind Follow-up duration: 6-10 days, mean 8 days Europe, Australia, South Africa |
dabigatran 220mg versus enoxaparin (US regimen) | |||
RE-MOBILIZE (220mg), 2008 | dabigatran etexilate 220 mg for 12-15 days
versus Enoxaparin 30mg SC BID after surgery for 12-15 days | Total knee replacement | double blind Follow-up duration: 12-15 days, median 14d US, Canada, Mexico, UK |
dalteparin versus Dextran | |||
Matzsch , 1991 | dalteparin versus Dextran | Elective hip | |
Eriksson , 1988 | dalteparin versus Dextran | Elective hip | |
Matzsch , 1988 | dalteparin versus Dextran | Elective hip | |
dalteparin versus placebo | |||
D-KAf (Selby), 2007 NCT00187408 | dalteparin 5000U daily versus placebo | below-knee fractures repaired surgically | |
Leizorovicz, 2004 | Dalteparin 5000E once daily, 1' days versus placebo | Congestive heart failure (NYHA III–IV), acute or chronic respiratory disease, infectious and rheumatologic disease | double blind Follow-up duration: 21 days |
Jorgensen, 1989 | dalteparin 5000 x1 versus Placebo | Hip fracture | double blind Follow-up duration: 9 days |
Torholm, 1991 | dalteparin 5000x1 versus Placebo | Elective hip | double blind Follow-up duration: 9 days |
Ockelford , 1989 | Dalteparin 2500 anti-Xa units versus Placebo | general surgery | Blind |
Lapidus, 2007 | Dalteparin 5000 IU versus Placebo | patients surgically treated for Achilles tendon rupture | double-blind Follow-up duration: 43 days |
Lapidus, 2007 | Dalteparin 5000 IU versus Placebo | patients undergoing ankle fracture surgery | double-blind Follow-up duration: 44 days |
dalteparin versus UFH | |||
PROTECT, 2011 NCT00182143 | subcutaneous dalteparin 5000 IU once daily versus unfractionated heparin 5000 IU twice daily | critically ill patients | double-blind Canada, Australia, Brazil, Saudi Arabia, US, UK |
Scala, 1990 | Dalteparin 120 IU/kg anti-Xa SC twice daily versus Standard heparin continuous IV infusion adaptedto maintain aPTTbetween 1.5 and2.5 times controlvalue | acute myocardial infarction | open Follow-up duration: 7 d |
dalteparin versus Unfractionated heparin | |||
Binsack , 1986 | dalteparin versus Unfractionated heparin | Elective hip | |
dalteparin versus unfractionated heparin | |||
Briel, 1988 | Dalteparin 5000 versus UFH 10 000 units+DHE | Gynaecological surgery | NA |
dalteparin versus Unfractionated heparin | |||
Barre , 1987 | dalteparin versus Unfractionated heparin | Elective hip | |
Dechavanne , 1989 | dalteparin versus Unfractionated heparin | Elective hip | |
dalteparin versus unfractionated heparin | |||
Bergqvist, 1986 | Dalteparin 5000 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 1 month |
Onarheim, 1986 | Dalteparin 5000 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 1 month |
dalteparin versus Unfractionated heparin | |||
Eriksson , 1989 | dalteparin versus Unfractionated heparin | Elective hip | |
Haas , 1985 | dalteparin versus Unfractionated heparin | Elective hip | |
dalteparin versus unfractionated heparin | |||
Koller, 1986 | Dalteparin 7500 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 30 days |
Koller, 1986 | Dalteparin 2500 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 30 days |
Fricker, 1988 | Dalteparin 5000 versus UFH 15 000 units | Abdominopelvic surgery | Open Follow-up duration: 1-2 months |
Bergqvist, 1988 | Dalteparin 5000 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 1 month |
Caen, 1988 | Dalteparin 2500 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: 1 month |
Borstad, 1988 | Dalteparin 5000 versus UFH 10 000 units | Gynaecological surgery | Blind |
dalteparin versus Unfractionated heparin | |||
Monreal , 1989 | dalteparin versus Unfractionated heparin | Hip | |
dalteparin versus unfractionated heparin | |||
Creperio, 1990 | Dalteparin 2500 versus UFH 10 000 units | General surgery | Blind |
Hartl, 1990 | Dalteparin 2500 versus UFH 10 000 units | Abdominal surgery | Blind Follow-up duration: > 7 days |
Borstad, 1992 | Dalteparin 2500 anti Xa units versus UFH 10 000 units | Gynaecological surgery | Blind |
Kakkar, 1993 | Dalteparin 2500 anti Xa units versus UFH 10 000 units | Abdominal surgery | Blind |
deltaparin versus control | |||
Michot, 2002 | deltaparin 2500IU 60-120min before procedure, followed 6hrs after the end of the procedure by 2500IU (<70kg) or 5000 IU(>70kg) versus no treatment | patients requiring diagnostic or therapeutic arthoscopic knee surgery as outpatients; aged18 to 80 years. | open Follow-up duration: 30 days Switzerland. |
desirudin versus enoxaparin | |||
Ericksson, 1997 | desirudin 15mg SC twice daily for 8-12 days versus enoxaparin 40mg once daily for 8-12 days | Patients who undergo total hip replacement | double blind Europe |
desirudin versus UFH | |||
REVASC, 1997 | desirudin 15mg twice daily versus unfractionated heparin 5000 IU three times a day | patients having a primary elective total hip replacement | |
Eriksson, 1996 | recombinant hirudin, desirudin (CGP 39393) 10, 15, or 20 mg twice daily started just before surgery and continued for 8-11 days versus unfractionated heparin 5000 IU three times daily started just before surgery and continued for 8-11 days | patients undergoing elective hip surgery | double blind Europe |
dipyridamol versus no treatment | |||
Morris-A , 1977 | dipyridamole versus control | elderly patients with hip fractures | open |
dipyridamol + ASA versus placebo | |||
Denver-Il , 1980 | dipyridamole 100 mg a day and aspirin 1200 mg a day versus placebo | patients with recurring venous thromboembolism | double-blind Follow-up duration: 18 months |
dipyridamol + aspirin versus control | |||
Parodi I, 1973 | Dip,A1000+Dip versus control | open | |
Parodi II, 1973 | A1500,Dip,A+Dip versus control | open | |
Australian I, 1975 | A1000+Dip versus control | open | |
Australian II, 1976 | A1000+Dip versus control | open | |
Toulouse I, 1979 | A990+Dip versus control | open | |
Zekert-III, 1977 | A1500,A1300+Dip,A1000+Dip versus control | open | |
Harjola DVT, 1982 | A1500,Dip,A+Dip versus control | open | |
Weiss, 1977 | A990+Dip versus control | open | |
dipyridamol + aspirin versus placebo | |||
Encke IA, 1976 | A990,A+Dip versus Placebo | double-blind | |
Encke IB, 1976 | A1500,A990+Dip versus Placebo | double-blind | |
edoxaban versus enoxaparin (short duration) | |||
STARS J-V, 0 NCT01181167 | edoxaban 30 mg once daily for 11 to 14 days versus subcutaneous enoxaparin 2,000 IU, equivalent to 20 mg, twice daily (BID) for 11 to 14 days | total hip arthroplasty | double-blind japan |
enoxaparin versus control | |||
Canata, 2003 | enoxaparin sc daily (dose not specified) versus no treatment | ACL reconstruction for symptomatic ACL-deficient knees | Follow-up duration: 6 days Italy |
enoxaparin versus Dextran | |||
DES Group , 1991 | Enoxaparin versus Dextran | Elective hip | |
enoxaparin versus no treatment | |||
Ho [43], | Enoxaparin 4000 anti-Xa units versus No treatment | Open | |
Warwick, 1995 | enoxaparin 4000x1 + elastic stockings versus no treatment + elastic stockings | Elective hip | open Follow-up duration: 8-10 days |
enoxaparin versus placebo | |||
LIFENOX, 2011 NCT00622648 | subcutaneous enoxaparin 40 mg daily for 10±4 days versus placebo | hospitalized, acutely ill medical patients | double-blind Follow-up duration: 30 days China, India, Korea, Malaysia, Mexico, the Philippines, and Tunisia |
Enoxaparin versus placebo | |||
Lederle, 2006 | Enoxaparin 40 mg once daily, until hospital discharge versus placebo | Hospitalization in general medical unit | double blind Follow-up duration: 90 days |
MEDENOX, 1999 | Enoxaparin 20 mg or 40 mg once daily, 6–14 days versus placebo | Acute decompensated chronic obstructive pulmonary disease with mechanical ventilation | double blind Follow-up duration: 6-14 days |
enoxaparin versus placebo | |||
Kalodiki, 1996 | enoxaparin 4000x1 versus Placebo | Elective hip | double blind Follow-up duration: discharge (8-12 days ) |
LeGagneux , 1987 | Enoxaparin 6000 anti-Xa units versus Placebo | prostatectomy surgery | Blind |
Leclerc, 1991 | Enoxaparin 3000 x2 versus Placebo | Knee | double blind Follow-up duration: 14 days |
Samama, 1997 | enoxaparin 4000x1+elastic stockings versus Placebo+elastic stockings | Elective hip | double blind Follow-up duration: 8-12 days |
Turpie, 1986 | Enoxaparin 3000 x2 versus Placebo | Elective hip | double blind Follow-up duration: 14 days or discharge |
Agnelli, 1998 | Enoxaparin, 40 mg/d subcutaneously within 24 hours postoperatively plus compression stockings for >=7 days versus compression stockings + placebo | Elective neurosurgery, 18 years or older, without excess bleeding risk | Follow-up duration: 30 days |
Melon, 1987 | Enoxaparin, 20 mg/d subcutaneously 18-24 hours postoperatively for 10 days versus placebo | Neurosurgery, adult, 45-90 kg of weight, without excess bleeding risk | Follow-up duration: NA |
enoxaparin versus UFH | |||
Bergmann and Neuhart, 1996 | enoxaparin 20 mg once daily for 10 days versus unfractionated heparin (UFH) 5000 IU twice daily | elderly in-patients bedridden for an acute medical illness | double-blind Follow-up duration: 10 days |
Lechler, 1996 | enoxaparin 40 mg versus unfractionated heparin (Ca-heparin), 3 x 5,000 U) | hospitalized medical patients | double-blind Follow-up duration: 7 days |
Kleber, 2003 | enoxaparin 40 mg once daily for 10 +/2 days versus UFH 5000 IU 3 times daily for 10 +/2 days | severe respiratory disease or heart failure | open Follow-up duration: 10 +/- 2 days Germany |
enoxaparin versus unfractionated heparin | |||
Samama 2, 1988 | Enoxaparin 4000 versus UFH 15 000 units | General surgery | Open Follow-up duration: 7 days |
Samama 1, 1988 | Enoxaparin 2000 versus UFH 15 000 units | General surgery | Open Follow-up duration: 7 days |
enoxaparin versus Unfractionated heparin | |||
Levine , 1991 | Enoxaparin versus Unfractionated heparin | Elective hip | |
enoxaparin versus unfractionated heparin | |||
Samama 3, 1988 | Enoxaparin 6000 versus UFH 15 000 units | General surgery | Open Follow-up duration: 7 days |
enoxaparin versus Unfractionated heparin | |||
Planes , 1988 | Enoxaparin versus Unfractionated heparin | Elective hip | |
enoxaparin versus unfractionated heparin | |||
Kaaja, 1992 | Enoxaparin 2000 anti Xa units versus UFH 10 000 units | Gynaecological surgery | Blind |
Gazzaniga (ISG), 1993 | Enoxaparin 2000 anti Xa units versus UFH 10 000 units | General and vascular surgery | Open |
Nurmohamed, 1995 | Enoxaparin 2000 anti Xa units versus UFH 15 000 units | General surgery | Blind |
McLeod (Canadian), 1995 | Enoxaparin 4000 anti Xa units versus UFH 15 000 units | Colorectal surgery | Blind |
Gonzalez, 1996 | Bemiparin 2500 anti Xa units versus UFH 10 000 units | Abdominal surgery | Blind |
ENOXACAN, 1997 | Enoxaparin 4000 anti Xa units versus UFH 15 000 units | Abdominopelvic surgery | Blind |
extended prophylaxis versus standard prophylaxis | |||
PENTHIFRA–PLUS (Eriksson), 2003 | 25-31 days of fondaparinux 2.5-mg once-daily versus 6-8 days of fondaparinux 2.5-mg once-daily | patients undergoing hip fracture surgery | double blind Follow-up duration: 19-23 days |
Lausen, 1998 | Tinzaparin 3500 UI/qd sc for 28 days started in preop versus Tinzaparin 3500 UI/qd + GES for 1 week started in preop | >18 years, open major abdominal surgery and non cardiac thoracic surgery of >1hour duration. | Open, blinded evaluation Follow-up duration: 28 days |
ENOXACAN II (Bergqvist), 2002 | Enoxaparin 40 mg UI/qd sc for 25-31 days started in preop versus Enoxaparin 40 mg IU/qd sc for 6 to 10 days (GES optional) started in preop | > 40 years, open major abdominal oncologic elective surgery of >45 minutes duration (includes gynecological surgery) | double blind Follow-up duration: 3 months |
FAME (Rasmussen), 2006 | Dalteparin 5000 UI/qd SC for 28 days started in preop versus Dalteparin 5000 UI/qd SC for 7 days + GES started in preop | > 18 years, major abdominal surgery of >1 hour duration | Open, blinded evaluation Follow-up duration: 3 months |
Extended-duration prophylaxis versus error | |||
EXCLAIM, 2010 NCT00077753 | Enoxaparin, 40 mg/d subcutaneously (for 28 +/-4 days after receiving openlabel
enoxaparin for an initial 10+/-4 days versus placebo for 28 +/-4 days after receiving openlabel enoxaparin for an initial 10+/-4 days. | Acutely Ill Medical Patients With Recently Reduced Mobility | double-blind Follow-up duration: 28 days North and South America |
extended-duration thromboprophylaxis versus standard-duration thromboprophylaxis | |||
Marlovits, 2007 | extended-duration thromboprophylaxis with enoxaparin for 20 days versus standard thromboprophylaxis with enoxaparin (3 to 8 days) | patients who had undergone arthroscopic surgery of the anterior cruciate ligament | double-blind Follow-up duration: <=28 days Austria |
Flurbiprofen versus no treatment | |||
Mocris-C , 1977 | Flurbiprofen versus control | elderly patients with hip fractures | open |
fluxum versus placebo | |||
Valle , 1988 | Parnaparin 3200 anti-Xa units versus Placebo | general surgery | Blind |
fluxum versus Unfractionated heparin | |||
Chiapuzzo , 1988 | Fluxum versus Unfractionated heparin | Elective hip | |
Pini , 1989 | Fluxum versus Unfractionated heparin | Hip | |
fondaparinux versus enoxaparin | |||
L8541, 0 | fondaparinux 2.5mg subcutaneous once-daily for 7+/-2 days versus enoxaparin 40mg s.c. once-daily | chinese patients undergoing major orthopaedic surgery of the lower limbs | single-blind Follow-up duration: 9 days (49d) China |
L8635, 0 | Fondaparinux 2.5mg once daily subcutaneously for 7 days versus enoxaparin 40mg once daily SC for 7 days | Taiwanese patients undergoing elective knee replacement | open, blind assessment Follow-up duration: 10 days Taiwan |
BRiEF, NCT00521885 | fondaparinux 2.5mg qd versus enoxaparin 40mg qd | acute medically ill, non-surgical patients | Germany |
PENTAMAKS (Bauer), 2001 | fondaparinux 2.5-mg once-daily subcutaneous, starting 6 hours after surgery versus enoxaparin 30mg twice daily (North america recommendation) | elective major knee surgery | double blind Follow-up duration: 11 days North america |
PENTHIFRA (Eriksson), 2001 | fondaparinux 2.5-mg once-daily subcutaneous, starting 6 hours after surgery versus enoxaprin 40mg once daily | hip fracture surgery | double blind Follow-up duration: 11 days 21 countries |
EPHESUS (Lassen), 2002 | fondaparinux 2.5-mg once-daily subcutaneous, starting 6 hours after surgery versus enoxaprin 40mg once daily | elective hip replacement surgery | double blind Follow-up duration: 11 days (6 weeks) 16 European countries |
PENTATHLON (Turpie), 2002 | fondaparinux 2.5-mg once-daily subcutaneous, starting 6 hours after surgery versus enoxaparin 30mg twice daily (North america recommendation) | elective hip replacement surgery | double blind Follow-up duration: 11 days USA, Canada, Australia |
PEGASUS, 2005 | once-daily subcutaneous injections of fondaparinux 2·5 mg started 6 h after surgery for 5–9 days versus once-daily subcutaneous injections of dalteparin 5000 units for 5–9 days (2500 units each, given 2 h before surgery and 12 h after the preoperative administration) | patients undergoing major abdominal surgery | double blind Follow-up duration: 10 days (30 days) 22 countries |
Turpie, 2001 | pentasaccharide Org31540/SR90107A subcutaneous once daily at doses 0.75 mg, 1.5 mg, 3.0 mg, 6.0 mg, and 8.0 mg versus enoxaparin 30mg once daily subcutaneous | patients undergoing total hip replacement | double blind Follow-up duration: >15 days US, Canada, Autralia |
fondaparinux versus placebo | |||
DRI4757, 0 | fondaparinux subcutaneously at 0.75, 1.5, 2.5, and 3.0 mg for at least 10 calendar days, (with a maximum of 14 days) versus placebo | Japanese patients undergoing elective total knee replacement surgery | double blind Follow-up duration: 14 days Japan |
ARTEMIS (Cohen), 2006 | Fondaparinux 2.5 mg once daily for 6–14 days versus placebo | High-risk medical patients | double blind Follow-up duration: 6-15 days 8 countries |
fondaparinux versus placebo (on top intermittent pneumatic comp.) | |||
APOLLO (Turpie), 2007 | fondaparinux 2.5 mg s.c. for 5-9 days, starting 6-8 h postoperatively + intermittent pneumatic compression versus placebo s.c. for 5-9 days, starting 6-8 h postoperatively + intermittent pneumatic compression | Patients aged at least 40 years undergoing abdominal surgery | double blind Follow-up duration: 10 days US |
Footpump versus LMWH | |||
Stone, 1996 | intermittent pneumatic calf compression versus Enoxaparin | total hip replacement | open |
Warwick, 1998 | A-V Impulse System foot pump versus LMWH | primary total hip replacement | open Follow-up duration: 8 days |
Blanchard, 1999 | continuous intermittent pneumatic compression of the foot by means of the arteriovenous impulse system versus one daily subcutaneous injection of nadroparin calcium (dosage adapted to body-weight) | patients undergoing total knee arthroplasty | open (blinded assessment) Follow-up duration: 12 days |
Footpump (adjunctive therapy) versus UFH then aspirin | |||
Stannard (vs UFH+asp), 1996 | intermittent pulsatile pneumatic-pump compression of the plantar venous plexus versus UFH followed by aspirin | patients undergoing elective total hip replacement arthroplasty | open |
Footpump (monotherapy) versus control | |||
Scurr, 1981 | Plantar flexion and dorsiflexion of the feet while the patient is on the operating table by the use of a mechanical device (the Pedi-Pulsor) versus control | abdominal or thoracic surgery | open |
Wilson, 1992 | versus | Elective knee remplacement | open |
GCS versus ??? | |||
Schirai, 1985 | versus | ||
GCS versus LMWH | |||
Camporese, 2008 | full-length graduated compression stocking for 7 days versus once-daily subcutaneous injection of LMWH (nadroparin, 3800 anti-Xa IU) for 7 days or 14 days | patients undergoing knee arthroscopy | open Italy |
GCS versus no prophylaxis | |||
Barnes, 1978 | graded-compression stockings versus nostockings | patients undergoing total hip replacement | |
*Inada, 1983 | graduated compression stocking on one leg versus no GCS on the other leg serving as a control. | patients undergoing major surgery | |
Rosengarten, 1970 | versus | ||
*Ohlund, 1983 | graded compression of the calf versus | elective total hip arthroplasty | |
*Wille-Jorgensen, 1989 | regional anesthesia and graded compression stockings versus general anesthesia | elective hip arthroplasty | |
*Tsapogas, 1971 | versus | ||
*Scurr, 1977 | graduated static compression stockings on one leg versus other leg being used as a control | patients undergoing Abdominal surgery | open |
Turner, 1984 | graduated compression stockings versus not wear the stockings | patients undergoing Gynecologic surgery | |
Allan, 1983 | graduated compression stockings versus control | patients undergoing Abdominal surgery | |
Turpie (GCS vs crtl), 1989 | graduated compression stockings versus untreated control | patients undergoing Neurosurgery surgery | |
Holford, 1976 | Graded compression versus control | patients undergoing major operations | |
CLOTS, 2009 | Thigh length graduated Compression Stockings versus no graduated Compression Stockings | Acute Stroke patients | open, blind asessor Follow-up duration: 30 days 3 countries |
GCS versus UFH | |||
Fasting, 1985 | graded compression stockings (TED stockings, Kendall Co.) versus low-dose heparin (Heparin Leo 5 000 I.U. subcutaneously twice daily) | elective major surgery | |
Hansberry (vs UFH), 1991 | thromboembolic stockings versus heparin plus dihydroergotamine | patients undergoing a major urological operation | Follow-up duration: 6 days |
Rasmussen (GCS vs UFH), 1998 | graduated compression stockings to the knee (TED stockings) versus subcutaneous heparin | patients (age more than 40 yrs) admitted for major abdominal surgery | open |
GCS + asp versus aspirin | |||
Muir, 2000 | graded compression stockings versus standard care alone | stroke | open (blinded assessment) |
Kierkegaard, 1993 | Graduated compression stockings were randomly fitted to one leg versus the otherleg serving as a control | myocardial infraction or ACS | |
GCS + dextran versus dextran | |||
*Bergqvist, 1984 | one leg encased in a graded compression stocking versus other leg unstockinged | patients undergoing Abdominal surgery | |
Fredin, 1989 | graded compression stockings + dextran versus dextran alone | patients undergoing THR surgery | |
GCS + LMWH versus LMWH | |||
Kalodiki (GCS+LMWH vs LMWH), 1996 | enoxaparin (40 mg once daily) plus graduated elastic compression (TEDR stockings) for 8-12 days versus low molecular weight heparin: (enoxaparin 40 mg once daily) | patients having elective total hip replacement | |
GCS + UFH versus UFH | |||
*Rasmussen (adj), 1988 | subcutaneous heparin and graduated compression stockings to the knee (TED stockings), versus subcutaneous heparin | patients (age more than 40 yrs) admitted for major abdominal surgery | open |
Torngren, 1980 | versus | ||
Wille-Jorgensen, 1985 | low-dose heparin treatment with graded compression stockings versus low-dose heparin treatment (5000 units twice daily subcutaneously) | patients undergoing Abdominal surgery | |
Wille-Jorgensen, 1991 | low dose heparin and graded compression stockings versus low dose heparin | patients undergoing Abdominal surgery | |
GCS +IPC versus IPC | |||
Mellbring, 1986 | graduated static compression + peroperative intermittent pneumatic calf compression versus peroperative intermittent pneumatic calf compression | patients undergoing major abdominal surgery | |
Scurr (GCS+IPC vs IPC), 1987 | simultaneous use of graduated compression stockings and intermittent sequential pneumatic compression versus intermittent sequential pneumatic compression | patients undergoing Abdominal surgery | |
Hydroxychloroquine versus no treatment | |||
Massachusetts-I , 1981 | Aspirin 1200mg daily, Aspirin 1200mg daily + hydroxychloroquine 300 mg b.i.d. versus control | patients with upper femoral fractures | open |
hydroxychloroquine versus placebo | |||
Carter IA, 1971 | Hydroxy versus placebo | double-blind | |
Hydroxychloroquine versus placebo | |||
Danish-A , 1976 | Hydroxychloroquine sulphate versus placebo | patients with fractures of the hip, pelvis, or thoracolumbar spine | double-blind |
hydroxychloroquine versus placebo | |||
Carter IB, 1971 | Hydroxy versus placebo | double-blind | |
Hydroxychloroquine versus placebo | |||
Danish-B , 1976 | Hydroxychloroquine sulphate versus placebo | patients with fractures of the hip, pelvis, or thoracolumbar spine | |
hydroxychloroquine versus placebo | |||
Carter II, 1974 | Hydroxy versus Placebo | double-blind | |
New York, 1977 | Hydroxy versus placebo | double-blind | |
Vermont, 1975 | Hydroxy versus placebo | double-blind | |
Hydroxychloroquine versus placebo | |||
Massachusetts-II, 1976 | Hydroxychloroquine 600mg daily versus placebo | fractures or orthopaedic operations involving the skeleton between the knee and the pelvis | Follow-up duration: 3 weeks |
Cooke, 1977 | Hydroxychloroquine versus placebo | elective surgery on the hip | double-blind Follow-up duration: 2 weeks |
Hume-A, 1977 | Hydroxychloroquine versus placebo | total hip replacement | Follow-up duration: 2 weeks |
Stockholm-II, 1981 | Hydroxychloroquine versus placebo | total hip replacement | Follow-up duration: 2 weeks |
IPC versus aspirin | |||
HAAS I, 1990 | versus | elective knee remplacement | open |
HAAS II, 1990 | versus | elective knee remplacement | open |
McKenna (vs aspirin), 1980 | versus | elective knee remplacement | open |
IPC versus DHE + low dose heparin | |||
Mellbring, 1986 | peroperative intermittent pneumatic calf compression versus dihydroergotamine (DHE) combined with low-dose heparin (LDH) | patients undergoing Abdominal surgery | open |
IPC versus LMWH | |||
Kurtoglu, 2004 | intermittent pneumatic compression versus LMWH | head/spinal traumatized patients | open Follow-up duration: 1 week after discharge Turkey |
Warwick à exclure, 2002 | IPCD/FID versus LMWH | open | |
Ginzburg, 2003 | intermittent pneumatic compression versus LMWH | Trauma patients >18 years old | open Follow-up duration: 30 days United States |
IPC versus UFH | |||
Clarke Pearson, 1993 | versus | open | |
Coe (vs UFH), 1978 | versus | open | |
Hansberry (vs UFH), 1991 | versus | open | |
Kosir, 1998 | versus | open | |
IPC versus vitamin K antagonists | |||
Chandhoke, 1992 | IPCD versus | major urological surgery | open |
paiement, 1987 | versus | elective hip replacement | open |
Kaempffe, 1991 | versus | elective hip & knee replacement | open |
IPC + aspirin versus aspirin | |||
Hull 2 (+asp), 1979 | versus | patients undergoing elective knee surgery | open |
Hull (+asp), 1979 | versus | patients undergoing elective knee surgery | open |
Lieberman (A), 1994 | hypotensive epidural anesthesia, external pneumatic-compression boots, and aspirin versus hypotensive epidural anesthesia and aspirin | primary unilateral or bilateral total hip arthroplasty with use of hypotensive epidural anesthesia | open |
IPC + dextran versus dextran | |||
Smith (D), 1978 | dextran 70 and pneumatic calf compression versus dextran 70 | open | |
IPC + GCS versus control | |||
Turpie, 1989 | graduated compression stockings plus intermittent pneumatic compression versus untreated control | potential neurosurgical patients | open Follow-up duration: 14 days |
IPC + GCS versus GCS | |||
Goldhaber, 1995 | intermittent pneumatic compression (IPC) plus graduated compression stockings (GCS) versus standard compression stockings alone | patients undergoing coronary artery bypass without concomitant valve surgery or coronary endarterectomy | open Follow-up duration: hospital stay |
Fordyce, 1992 | venous foot pump (A-V Impulse System) versus control | elective hip replacement | open |
Rokito, 1996 | TED stockings and thigh-length cuffs that provided sequential pneumatic compression to the calf and thigh versus bilateral thigh-high thrombosis embolic deterrent (TED) compression stockings (Kendall Company, MA). | neurosurgery | open |
Turpie, 1989 | graduated compression stockings plus intermittent pneumatic compression versus graduated compression stockings alone | neurosurgery | open Follow-up duration: 14 days |
Wautrecht, 1996 | versus | neurosurgery | open |
Caprini, 1983 | versus | general surgery | open |
Lacut, 2005 | elastic stockings combined with intermittent pneumatic compression versus elastic stockings alone | patients with a documented intracerebral hemorrhage | open Follow-up duration: 1à days |
Pambianco, 1995 | versus | stroke | open |
IPC + GCS versus LMWH | |||
Norgren, 1998 | IPCD/FID + GCS versus LMWH | elective knee remplacement | open |
IPC + GCS versus UFH | |||
Niolaides, 1983 | IPCD + GCS versus UFH | general surgery | open |
Santori, 1994 | IPC + GCS versus UFH | elective hip replacement | open |
IPC + GCS +LMWH versus GCS +LMWH | |||
Dickinson, 1998 | sequential compression device +enoxaparin (+ GCS) versus enoxaparin (+GCS) | neurosurgery, patients with brain tumors | open Follow-up duration: 1 month |
IPC + UFH versus control | |||
Killewich, 1997 | low-dose heparin sodium therapy (5000 U every 12 hours) and calf-length intermittent mechanical compression devices versus no prophylaxis | patients undergoing aortic reconstruction for aneurysmal or occlusive disease | open |
IPC + UFH versus UFH | |||
Ramos, 1996 | prophylactic regimen of Pneumatic compression stocking and subcutaneous heparin versus with 5,000 U of subcutaneous heparin every 12 h | cardiac surgery | open |
Siragusa (H), 1994 | versus | open | |
IPC – sequential compression versus control | |||
Blackshear à exclure, 1987 | Sequential external pneumatic compression versus control | abdominal or thoracic surgery | open |
Hull II, 1990 | sequential intermittent calf and thigh compression versus no prophylaxis | patients undergoing total hip replacement | open |
Fisher, 1995 | pneumatic sequential leg compression devices versus no specific form of prophylaxis | orthopaedic trauma patients with hip and pelvic fractures | open |
Turple II, 1979 | intermittent sequential calf compression versus | patients with intracranial disease | open |
Knudson, 1994 | sequential gradient pneumatic leg compression versus control | trauma patients | open |
Kosir, 1996 | sequential pneumatic compression devices during surgery and 2 days postoperatively versus control | Patients undergoing procedures of at least 1 hr duration (abdominal, thoracic, head and neck, inguinal) requiring general or spinal anesthetic | open Follow-up duration: 30 days |
IPC – sequential compression versus Footpump | |||
Elliott, 1999 | Calf-thigh sequential pneumatic compression versus foot pump (plantar venous pneumatic compression) | Trauma patients >13 years old | open (blind assessement) Follow-up duration: NA United States |
IPC – single compression versus control | |||
Prasad, 1982 | pneumatic compression of the calf versus No Prophylaxis | elderly hemiplegics | open |
Butson, 1981 | intermittent pneumatic calf compression, begun after the induction of anesthesia and continued until the patient was walking versus control | patients undergoing major abdominal general surgical procedures | open |
Clark, 1974 | Pneumatic compression of the calf versus | abdominal or thoracic surgery | open |
Clarke-Pearson I, 1984 | versus | open | |
Clarke-Pearson II, 1984 | versus | abdominal or thoracic surgery | open |
Coe, 1978 | low-dose heparin and external pneumatic compression (EPC) of the calves versus no treatment | patients undergoing open urological operations | open |
Hills, 1972 | intermittent pneumatic compression of calf versus | abdominal or thoracic surgery | open |
Gallus, 1983 | preventive intermittent calf compression versus no prophylaxis | elective hip replacement | open Follow-up duration: in hospital |
Bachmann, 1976 | low pressure intermittent compression (Phlebo-Dynastat) to calves and thighs started on the day of operation and continued until patients were fully mobilized versus | patients undergoing joint-replacement operations | open Follow-up duration: until patients fully mobilized |
Bynke, 1987 | versus | neurosurgery | open |
Skillman, 1978 | external pneumatic compression (EPC) of the calves versus no specific form of prophylaxis | patients undergoing neurosurgical operative procedures | open Follow-up duration: NA |
Turpie I, 1977 | intermittent pneumatic compression of the calf versus | patients with intracranial disease | open |
Hull I, 1979 | intermittent pulsatile elastic stockings versus | patients undergoing elective knee surgery | open |
IPC – unknown type versus control | |||
Weitz, 1986 | intermittent pneumatic calf compression versus | open | |
IPC/FID versus GES | |||
Hansberry, 1991 | versus | open | |
IPCD versus control | |||
McKenna, 1980 | IPCD versus No Prophylaxis | Elective knee remplacement | open |
IPD or GCS versus no prophylaxis | |||
Turpie (IPD or GCS), 1989 | versus | ||
Knee length GCS versus Thigh length GCS | |||
Hui THR, 1996 | Knee length GCS versus Thigh length GCS | Orthopaedic patients THR | |
Hui TKR, 1996 | Knee length GCS versus Thigh length GCS | Orthopaedic patients TKR | |
William, 1996 | Knee-length graduated compression stockings versus thigh-length graduated compression stoc | orthopaedic surgery | |
Porteous, 1989 | Knee length GCS versus Thigh length GCS | General surgical patients | |
Williams, 1988 | Knee length GCS versus Thigh length GCS | General surgical patients | |
Howard, 2004 | Knee length GCS versus Thigh length GCS | Breast surgery, oncology, ENT, urology, vascular, neurosurgery. And gastrointestinal surgery | |
LMWH versus UFH | |||
Harenberg, 1990 | 1 x 1.500 aPTT units of a LMW heparin fraction versus 3 x 5.000 IU of an unfractionated heparin | patients aged 40-80 years | double-blind Follow-up duration: 10 days |
Harenberg, 1996 | 1 daily subcutaneous administration of LMW heparin for 10 days versus 3 x 5,000 IU unfractionated (UF) heparin for 10 days | medical inpatients | double-blind Follow-up duration: 10 days |
nadroparin versus control | |||
KANT (7 days), 2008 | once-daily subcutaneous injection of LMWH (nadroparin, 3800 anti-Xa IU) for 7 days versus full-length graduated compression stocking for 7 days | patients undergoing knee arthroscopy | open (blinded assessment) Follow-up duration: 3 months Italy |
Roth, 1995 | 0.3 ml sc fraxiparine 2 hours before the operation and self administered daily (except the firstvtwo doses) for 4 days after surgeryn/x versus no treatment | patients undergoing ambulatory arthroscopic | Follow-up duration: 4 days Germany |
Kujath, 1993 | Nadroparin 2850 IU versus no prophylaxis | patients with injuries of the lower limb immobilized by a plaster cast | open Follow-up duration: 16 days |
nadroparin versus enoxaparin | |||
FX140, Simonneau G, 2006 | versus | ||
nadroparin versus no treatment | |||
Marassi [41], | Nadroparin 2850 anti-Xa units versus No treatment | Open | |
Yoo, 1997 | nadroparin 41/kgx1 days 1-3, 62/kg x1 days 4-11+elastic stockings versus no treatment | Elective hip | open Follow-up duration: 10 days |
nadroparin versus placebo | |||
Bergmann, 1996 | nadroparin 7500 u anti-Xa once daily versus placebo | hospitalized medical | Follow-up duration: up to 21 |
Balas [40], | Nadroparin 2850 anti-Xa units versus Placebo | Blind | |
Nadroparin versus placebo | |||
Fraisse, 2000 | Nadroparin 3800–5700E once daily, Until no longer mechanical ventilation, <=21 days versus placebo | Acute decompensated chronic obstructive pulmonary diseasewith mechanical ventilation | double blind Follow-up duration: <=21 days |
Mahe, 2005 | nadroparin 7500E once daily, Until hospital discharge, <=21 days versus placebo | Congestive heart failure (NYHA III–IV), acute or respiratory disease, nonpulmonary sepsis, cancer | double blind Follow-up duration: <=21 days |
nadroparin versus placebo | |||
Sourmelis, 1995 | nadroparin 3075x1 preop, 6150x1 post op versus Placebo | Hip fracture | double blind Follow-up duration: 10-12 days |
Pezzuoli, 1989 | Nadroparin 2850 anti-Xa units versus Placebo | general surgery | Blind |
Nurmohamed, 1996 | Nadroparin, 7500 Institute Choay anti-Xa units per day subcutaneously 18-24 hours postoperatively plus compression for 10 days versus compression stockings + placebo | Craniotomy or spinal surgery for tumor or injury, 18 years or older, without excess bleeding risk | Follow-up duration: 56 days |
nadroparin versus unfractionated heparin | |||
Kakkar and Murray, 1985 | Nadroparin 2850 versus UFH 10 000 units | General surgery | Blind Follow-up duration: 10 days |
EFS, 1988 | Nadroparin 2850 versus UFH 15 000 units | Abdominal surgery | Open Follow-up duration: 1 month |
nadroparin versus Unfractionated heparin | |||
Leyvraz, 1991 | Fraxiparin versus Unfractionated heparin | Elective hip | |
nadroparin versus unfractionated heparin | |||
Dahan, 1989 | Nadroparin 2850 versus UFH 15 000 units | Thoracic surgery | Open |
Barbui, 1990 | Nadroparin 2850 anti Xa units versus UFH 10 000 units | General surgery | Open |
Eurin, 1994 | Nadroparin 2850 anti Xa units versus UFH 15 000 units | Abdominopelvic surgery | Open |
nadroparin 14d versus control | |||
KANT (14 days), 2008 | once-daily subcutaneous injection of LMWH (nadroparin, 3800 anti-Xa IU) for 14 days versus full-length graduated compression stocking for 7 days | patients undergoing knee arthroscopy | open (blinded assessment) Follow-up duration: 3 months Italy |
out of hospital Ardeparin versus standard prophylaxis | |||
Heit, 2000 | in hospital thromboprophylaxis followed by out of hospital Ardeparin 100 IU/kg once a day for a total duration of 42 days versus Ardeparin 50 IU/kg twice a day for 4-10 days | THR or TKR | |
out of hospital Dalteparin versus standard prophylaxis | |||
Dahl, 1997 | in hospital thromboprophylaxis followed by out of hospital Dalteparin 5000 IU once a day for a total duration of 35 days versus Dalteparin 5000 IU once a day for 7 days (dextran day 0 and day 1) | THR | |
Lassen, 1998 | in hospital thromboprophylaxis followed by out of hospital Dalteparin 5000 IU once a day for a total duration of 35 days versus Dalteparin 5000 IU once a day for 7 days | THR | |
Hull, 2000 | in hospital thromboprophylaxis followed by out of hospital Dalteparin 5000 IU once a day for a total duration of 35 days versus Dalteparin 5000 IU once a day or warfarin for 6 days | THR | |
out of hospital Enoxaparin versus standard prophylaxis | |||
Bergqvist, 1996 | in hospital thromboprophylaxis followed by out of hospital Enoxaparin 40 mg once a day for a total duration of 30 days versus Enoxaparin 40 mg once a day for 10-11 days | THR | |
Planes, 1996 | in hospital thromboprophylaxis followed by out of hospital Enoxaparin 40 mg once a day for a total duration of 35 days versus Enoxaparin 40 mg once a day for 13-15 days | THR | |
Comp, 2001 | in hospital thromboprophylaxis followed by out of hospital Enoxaparin 40 mg once a day for a total duration of 27-29 days versus Enoxaparin 30 mg twice a day for 7-10 days | THR or TKR | |
out of hospital Nadroparin versus standard prophylaxis | |||
NPHDO, 1998 | in hospital thromboprophylaxis followed by out of hospital Nadroparin weight-adjusted for a total duration of 37-38 days versus Nadroparin weight-adjusted for 16-17 days | THR | |
out of hospital UFH versus standard prophylaxis | |||
Manganelli, 1998 | in hospital thromboprophylaxis followed by out of hospital UFH 5000 IU three times a day for a total duration of 30 days versus UFH 5000 IU three times a day for 15 days | THR | |
parnaparin versus unfractionated heparin | |||
Catania, 1988 | Parnaparin 3200 versus UFH 15 000 units | Abdominal surgery | Open |
Salcuni, 1988 | Parnaparin 3200 versus UFH 15 000 units | Abdominal surgery | Open |
Verardi, 1989 | Parnaparin 6400 versus UFH 10 000 units | Abdominal/urological surgery | NA |
Garcea, 1992 | Parnaparin 3200 anti Xa units versus UFH 15 000 units | Abdominal surgery | Open |
Pharmuka versus placebo | |||
Dahan, 1986 | Pharmuka 60 mg once daily, Until hospital discharge,<=10 days versus placebo | Congestive heart failure (NYHA III–IV), acute or respiratory infectious disease | double blind Follow-up duration: <10 days |
Phenindione versus no treatment | |||
Eskeland, 1966 | Phenindione versus No treatment | HFS | Open Follow-up duration: 3 months |
Hamilton, 1970 | Phenindione versus No treatment | HFS | Open Follow-up duration: 3–10 months |
RA233 versus placebo | |||
Wood , 1973 | RA233; Aspirin 600mg daily +RA233 versus placebo | traumatic orthopaedic surgery | |
reviparin versus control | |||
Wirth, 2001 | reviparin 1,750 anti Xa IU Sc once daily for 7-10 days versus no treatment | elective knee arthroscopy | open (blind assessement) Follow-up duration: 7-10 days Germany |
reviparin versus placebo | |||
Lassen, 2002 | Reviparin 1750 IU versus Placebo | patients who required immobilization in a plaster cast or brace for at least five weeks after a leg fracture or rupture of the Achilles tendon | double-blind Follow-up duration: 43 days |
reviparin versus unfractionated heparin | |||
Kakkar, 1993 | Reviparin 1750 anti Xa units versus UFH 10 000 units | General and gynaecological surgery | Blind |
rivaroxaban versus enoxaparin | |||
RECORD 1, 2008 NCT00329628 | rivaroxaban 10mg once daily for 35 days versus enoxaparin 40mg subcutaneous once daily for 31-39 days | patients undergoing total hip arthroplasty | double blind Follow-up duration: 36 days (range 30-42) 27 countries worldwide |
rivaroxaban versus enoxaparin (europe regimen) | |||
RECORD 3, 2008 NCT00361894 | rivaroxaban 10 mg once daily for 10- 14 days versus enoxaparin 40 mg subcutaneous once daily for 10-14 days | patients undergoing total knee arthroplasty | double blind Follow-up duration: 13-17 days 19 countries worldwide |
rivaroxaban versus enoxaparin (short duration) | |||
ODIXa-HIP 10mg, 2006 | rivaroxaban 10mg daily for 5–9 days versus once-daily subcutaneous enoxaparin dose of 40 mg for 5–9 days | patients undergoing elective total hip replacement | double blind Follow-up duration: 5-9 days Europe, Israel |
rivaroxaban versus enoxaparin (US regimen) | |||
ODIXa-KNEE, 2005 | BAY 59-7939 5mg b.i.d. for 5–9 days versus enoxaparin 30 mg b.i.d. for 5–9 days | patients undergoing elective total knee replacement | double blind Follow-up duration: 5-9 days North America |
RECORD 4, 2009 NCT00362232 | rivaroxaban 10mg once daily for 10 to 14 days versus enoxaparin 30 mg twice daily by subcutaneous injection for 10-14 days | patients who had undergone total-knee-replacement surgery | double blind Follow-up duration: 40 days 12 countries |
rivaroxaban versus placebo | |||
MARINER, 2018 NCT02111564 | once-daily rivaroxaban at a dose of 10 mg (with the dose adjusted for renal insufficiency) , begun at hospital discharge and continued for 45 days versus placebo | high-risk medical patients : medically ill patients who were at increasedrisk for venous thromboembolism on the basis of a modified International Medical Prevention Registry on Venous Thromboembolism (IMPROVE) score of 4 or higher (scores range from 0 to 10, with higher scores indicating a higher risk of venous thromboembolism) or a score of 2 or 3 plus a plasma d-dimer level of more than twice the upper limit of the normal range (defined according to local laboratory criteria) | double blind |
rivaroxaban (long duration) versus enoxaparin (short duration) | |||
RECORD 2, 2008 NCT00332020 | extended thromboprophylaxis with rivaroxaban 10mg once daily for 31-39 days versus enoxaparin 40mg subcutaneous once daily for 10-14 days | patients undergoing elective total hip replacement | double blind Follow-up duration: 30-42 days 21 countries worldwide |
semuloparin versus enoxaparin | |||
SAVE-HIP1, 2012 NCT00697099 | Semuloparin 20 mg once-daily versus Enoxaparin 40 mg once-daily | ||
SAVE-KNEE, 2012 NCT00718224 | Semuloparin 20 mg once-daily versus Enoxaparin 30 mg twice-daily | ||
SAVE-HIP 2, 2012 NCT00721760 | Semuloparin 20 mg once-daily versus Enoxaparin 40 mg once-daily | hip fracture surgery | |
sp versus control | |||
Veth, 1985 | Sp+Hep v Hep versus control | open | |
sp versus placebo | |||
Athens, 1981 | Sp versus placebo | double-blind | |
SR123781A versus enoxaparin | |||
DRIVE, 2008 NCT00338897 | SR123781A for 5-10 days, doses ranging from 0.25 to 4.0 mg daily for 10 days versus enoxaparin 40 mg | patients undergoing total hip replacement surgery | double blind Follow-up duration: 5-10 days 12 countries |
SSHA versus unfractionated heparin | |||
ToÈrngren, 1984 | SSHA 50 mg and 37.5 mg versus UFH 10 000 units | General surgery | Blind Follow-up duration: Discharge |
Suloctidil versus placebo | |||
Turpie, 1985 | Suloctidil versus Placebo | double-blind | |
thigh Length IPCD versus calf Length IPCD | |||
Soderdahl, 1997 | Thigh Length IPCD versus Calf Length IPCD | patients undergoing major urological surgery | open Follow-up duration: in hospital |
ticlopidine versus placebo | |||
Lasierra, 1982 | Ticlopidine versus placebo | double-blind | |
Walker, 1974 | ticlopidine versus placebo | double-blind | |
Ticlopidine versus placebo | |||
McKenna-II, 1983 | Ticlopidine versus placebo | Elective orthopaedic surgery | Follow-up duration: 2 weeks |
Lyon-II, 3000 | Ticlopidine versus placebo | Elective orthopaedic surgery | Follow-up duration: 3 weeks |
Gardecki, 3000 | Ticlopidine versus placebo | Elective orthopaedic surgery | Follow-up duration: 2 weeks |
ticlopidine versus placebo | |||
McKenna-II , 1983 | Ticlopidine versus placebo | high risk (post CVA) medical patients | double-blind |
tinzaparin versus control | |||
Jorgensen, 2002 | Tinzaparin 3500 IU versus no prophylaxis | patients over 18 years of age with planned plaster cast on a lower extremity of at least 3 weeks | open, assessor-blinded Follow-up duration: 38 days |
tinzaparin versus placebo | |||
Bergqvist [42], | Tinzaparin 3500 anti-Xa units versus Placebo | Blind | |
Lassen, 1991 | tinzaparin 50/kg x1 +elastic stockings versus Placebo+elastic stockings | Elective hip | double blind Follow-up duration: 8-10 days |
tinzaparin versus unfractionated heparin | |||
Leizorovicz, 1991 | Tinzaparin 2500 and 3500 anti Xa units versus UFH 10 000 units | Abdominothoracic and gynaecological surgery | Blind |
UFH versus aspirin | |||
Loew, 1977 | UFH twice daily for 7 days versus aspirin | all other general surgery | |
Vinazzer, 1980 | UFH twice daily for A days versus aspirin | all other general surgery | |
UFH versus control | |||
Handley, 1972 | Heparin 5000 U IV (loading dose) followed by 20 000 U IV twice daily versus no heparin | Myocardial infarction | Follow-up duration: 14 d |
Handley (low dose), 1972 | Heparin 5000 U IV and 7500 U SC as soon as possible, then 7500 U SC twice daily versus no heparin | Myocardial infarction | Follow-up duration: 7 d |
Blech, 1981 | Unfractionated heparin, 5000 U trice daily, until mobilized versus control | Heart failure, chest infection | open Follow-up duration: <=14 days |
Gallus, 1973 | heparin 5000 U SC 3 times daily versus no heparin | Myocardial infarction | Follow-up duration: until mobile |
Cade, 0 | Unfractionated heparin, 5000 U twice daily, until mobilized or <=10 days versus | Age >40, complete bed rest, cardiac failure, obesity, previous VTE, cancer or recent surgery | Follow-up duration: <=10 days |
Warlow, 1973 | Heparin sodium 5000 U SC twice dailyly versus no heparin | Myocardial infarction | double blind Follow-up duration: 10 d |
Gardlund, 1996 | Unfractionated heparin, 5000 U twice daily, until hospital discharge, <=21 days versus control | Age >55, infectious disease Immobilization | open Follow-up duration: <=60 days |
Emerson, 1973 | Heparin Low dose SCium9 versus no heparin | Myocardial infarction | Follow-up duration: NA |
Zawilska, 1989 | Heparin sodium 5000 IU SC twice dailyy for 14 to 21 days versus no heparin | patients with acute myocardial infarction, disqualified for thrombolytic treatment | Follow-up duration: 14-21 d |
UFH versus DHE | |||
Muiticentre, 1984 | UFH twice daily for 5-7 days versus DHE | all other general surgery | |
Muiticentre 53,S4, 1984 | UFH twice daily for 5-7 days versus DHE | all other general surgery | |
UFH versus no treatment | |||
Abernethy, 1974 | UFH twice daily for 7 days versus no treatment | all other general surgery | |
Abraham-Inpijn, 1979 | UFH twice daily for 7 days versus no treatment | all other general surgery | |
Allen, 1978 | UFH twice daily for D versus no treatment | urologic surgery | |
Bergqvist , 1979 | UFH twice daily for 5 days versus no treatment | elective orthopedic surgery | |
Bergqvist, 1979 | UFH twice daily for 5 days versus no treatment | traumatic orthopedic surgery | |
Bergqvist, 1980 | UFH twice daily for 5 days versus no treatment | all other general surgery | |
Caloghera, 1984 | UFH 3 times daily for 7 days versus no treatment | all other general surgery | |
Clarke-Pearson, 1983 | UFH twice daily for 7 days versus no treatment | all other general surgery | |
Coe, 1978 | UFH twice daily for D versus no treatment | urologic surgery | |
Dechavanne, 1974 | UFH 3 times daily for 10 days versus no treatment | elective orthopedic surgery | |
Dechavanne, 1975 | UFH 3 times daily for 10 days versus no treatment | elective orthopedic surgery | |
Galasko , 1976 | UFH twice daily (duration unknown) versus no treatment | traumatic orthopedic surgery | |
Gallus , 1973 | UFH 3 times daily for A versus no treatment | traumatic orthopedic surgery | |
Gallus , 1973 | UFH twice daily for A days versus no treatment | elective orthopedic surgery | |
Gallus, 1973 | UFH 3 times daily for A versus no treatment | all other general surgery | |
Gallus, 1976 | UFH 3 times daily for 7 days versus no treatment | all other general surgery | |
Gordon-Smith, 1972 | UFH twice daily for 5 days versus no treatment | all other general surgery | |
Groote Schuur, 1979 | UFH 3 times daily for 6 days versus no treatment | all other general surgery | |
Gruber, 0 | UFH 3 times daily for 7 days versus no treatment | All other general surgery | |
Kakkar (IMT), 0 | UFH 3 times daily for 7 days versus no treatment | All other general surgery | |
Kettunen, 1974 | UFH 3 times daily for 7 days versus no treatment | all other general surgery | |
Koppenhagen, 1982 | UFH twice daily versus no treatment | all other general surgery | |
Kraytman, 1976 | UFH 3 times daily for 6 days versus no treatment | all other general surgery | |
Kraytman, 1977 | UFH 3 times daily for 6 days versus no treatment | all other general surgery | |
Mannucci , 1976 | UFH 3 times daily for 7 days versus no treatment | elective orthopedic surgery | |
Marchelli, 1983 | UFH 3 times daily for ? versus no treatment | all other general surgery | |
Morris, 1974 | UFH twice daily for 10 days versus no treatment | elective orthopedic surgery | |
Morris , 1977 | UFH 3 times daily for 10 days versus no treatment | traumatic orthopedic surgery | |
Multiunit, 1974 | UFH twice daily for 7 days versus no treatment | all other general surgery | |
Nicolaides, 1972 | UFH twice daily for 7 days versus no treatment | all other general surgery | |
Plante, 1979 | UFH twice daily for 8 days versus no treatment | all other general surgery | |
Sagar, 1974 | UFH twice daily for 5 days versus no treatment | all other general surgery | |
Sebeseri, 1975 | UFH twice daily for D versus no treatment | urologic surgery | |
Spebar, 1981 | UFH twice daily for 5-7 days versus no treatment | all other general surgery | |
VTCSG, 1975 | UFH twice daily for 10 days versus no treatment | elective orthopedic surgery | |
Welin-Berger, 1982 | UFH twice daily for 7 days versus no treatment | elective orthopedic surgery | |
Ziemski, 1979 | UFH 3 times daily for 2 days versus no treatment | all other general surgery | |
Cerrato, 1978 | Unfractionated heparin, 5000 IU subcutaneously 3 times a day, starting 2 hours preoperatively for +7 days versus no treatment | Elective neurosurgery for tumors, 40 years or older | Follow-up duration: NA |
UFH versus oral anticoagulant | |||
van Geloven, 1977 | UFH twice daily for 4 days versus Oral anticoagulant | all other general surgery | |
UFH versus placebo | |||
Abraham-Inpijn , 1975 | UFH twice daily for 8 days versus placebo | elective orthopedic surgery | |
Bejjani, 1983 | UFH twice daily for 2 days versus placebo | urologic surgery | |
Belch, 1980 | UFH twice daily for 7 days versus placebo | all other general surgery | |
Pitt, 1980 | Heparin 500 U IV twice daily versus placebo | patients with acute myocardial infarction of less than 48 hours duration | open Follow-up duration: 2-3 d |
Covey, 1975 | UFH twice daily for 8 days versus placebo | all other general surgery | |
Hampson, 1974 | UFH 3 times daily for 7- 10 days versus placebo | elective orthopedic surgery | |
Hedlund, 1979 | UFH 3 times daily for 5 days versus placebo | urologic surgery | |
Jourdan, 1984 | UFH twice daily for 5 days versus placebo | all other general surgery | |
Kakkar, 1972 | UFH twice daily for 7 days versus placebo | All other general surgery | |
Kiil, 1978 | UFH twice daily for 7 days versus placebo | All other general surgery | |
Kraytman, 1977 | UFH 3 times daily for 6 days versus placebo | all other general surgery | |
Kruse-Blinkenberg, 1980 | UFH 3 times daily for 8 days versus placebo | all other general surgery | |
Kutnowski, 1977 | UFH 3 times daily for 6 days versus placebo | urologic surgery | |
Lahnborg, 1975 | UFH twice daily for 5 days versus placebo | all other general surgery | |
Lahnborg, 1976 | UFH twice daily for 5 days versus placebo | all other general surgery | |
Lahnborg, 1980 | UFH twice daily for 10 days versus placebo | traumatic orthopedic surgery | |
Lawrence, 1977 | UFH twice daily for 5 days versus placebo | all other general surgery | |
Lowe , 1981 | UFH twice daily for 16 days versus placebo | elective orthopedic surgery | |
Marchetti, 1982 | UFH 3 times daily versus placebo | all other general surgery | |
Moskovitz, 1978 | UFH 3 times daily for 7 days versus placebo | traumatic orthopedic surgery | |
Moskovitz, 1978 | UFH 3 times daily for 7 days versus placebo | elective orthopedic surgery | |
Muiticentre, 1984 | UFH twice daily for 5-7 days versus placebo | all other general surgery | |
Ribaudo, 1975 | UFH twice daily for A days versus placebo | all other general surgery | |
Roberts, 1975 | UFH twice daily for 7 days versus placebo | all other general surgery | |
Strand, 1975 | UFH twice daily for 7 days versus placebo | all other general surgery | |
Svend-Hansen, 1981 | UFH 3 times daily for 14 days versus placebo | traumatic orthopedic surgery | |
Taberner, 1978 | UFH twice daily for 7 days versus placebo | all other general surgery | |
Torngren, 0 | UFH twice daily for 6-8 days versus placebo | all other general surgery | |
Torngren, 1978 | UFH 3 times daily for 6-8 days versus placebo | all other general surgery | |
Torngren, 1978 | UFH twice daily for 6-8 days versus placebo | all other general surgery | |
Vandendris, 1980 | UFH 3 times daily for 6 days versus placebo | urologic surgery | |
Williams , 1978 | UFH twice daily for 14 days versus placebo | elective orthopedic surgery | |
Wu, 1977 | UFH twice daily for 7 days versus placebo | all other general surgery | |
Xabregas , 1977 | UFH twice daily for 14 days versus placebo | traumatic orthopedic surgery | |
Warfarin versus Ardeparin | |||
RD Heparin, 1994 | Warfarin versus Ardeparin 50 anti-Xa IU /kg or 90 anti-Xa IU /kg x1 | THR or TKR | Open Follow-up duration: 3 months |
Heit, 1997 | Warfarin versus Ardeparin 25, 35, 50 anti-Xa U /kg x2 | TKR | double blind Follow-up duration: Days 5–14 |
Warfarin versus Aspirin | |||
Lotke, 1997 | Warfarin versus Aspirin 325 mg x2 | THR or TKR (stratified) | Open Follow-up duration: 6 months |
Powers, 1989 | Warfarin versus Aspirin 650 mg x2 | HFS | Open Follow-up duration: 3 months |
Warfarin versus Dalteparin | |||
Francis, 1997 | Warfarin versus Dalteparin 5000 anti-Xa IU x1 | THR | Open Follow-up duration: Day 7 ± 2 |
Hull, 2000 | Warfarin versus Dalteparin 5000 anti-Xa IU x1 | THR | double blind Follow-up duration: Day 6 ± 2 |
Warfarin versus Danaparoid | |||
Gerhart, 1991 | Warfarin versus Danaparoid 750 U x2 | HFS | Open Follow-up duration: 9 days |
van Comp, 1998 | Warfarin versus Danaparoid 750 U x2 | THR | Open Follow-up duration: 3 months |
Warfarin versus Dextran | |||
Harris, 1972 | Warfarin versus Dextran 40 | THR | Open Follow-up duration: NA |
Barber, 1977 | Warfarin versus Dextran 70 | THR | Open Follow-up duration: 11–14 days |
Francis, 1983 | Warfarin versus Dextran 40 | THR or TKR (stratified) | Open Follow-up duration: 5–7 days |
Myrhe, 1969 | Warfarin versus Dextran 70 | HFS | double blind Follow-up duration: 3 weeks |
Warfarin versus Enoxaparin | |||
Leclerc, 1996 | Warfarin versus Enoxaparin 30 mg x2 | TKR | double blind Follow-up duration: 6 months |
Colwell, 1999 | Warfarin versus Enoxaparin 30 mg x2 | THR | Open Follow-up duration: 3 months |
Fitzgerald, 2001 | Warfarin versus Enoxaparin 30 mg x2 | TKR | Open Follow-up duration: 3 weeks |
Warfarin versus Intermittent pneumatic compression | |||
Francis, 1992 | Warfarin versus IPC | THR | Open Follow-up duration: 6–8 days |
Paiement, 1987 | Warfarin versus IPC | THR | Open Follow-up duration: 12 days |
Bailey, 1991 | Warfarin versus IPC | THR | Open Follow-up duration: 5–7 days |
Kaempffe, 1991 | Warfarin versus IPC | THR or TKR (stratified) | Open Follow-up duration: At least 2 months |
Warfarin versus Logiparin | |||
Hull, 1993 | Warfarin versus Logiparin 75 anti-Xa IU /kg x1 | THR or TKR (stratified) | double blind Follow-up duration: Day 14 or discharge |
Warfarin versus no treatment | |||
Pinto, 1970 | Warfarin versus No treatment | Hip surgery | Open Follow-up duration: > 3 weeks |
Hume, 1973 | Warfarin versus No treatment | THR | Open Follow-up duration: Discharge |
Morris, 1976 | Warfarin versus No treatment | HFS | Open Follow-up duration: 3 months |
Powers, 1989 | Warfarin versus No treatment | HFS | Open Follow-up duration: 3 months |
Warfarin versus placebo | |||
Myrhe, 1969 | Wwarfarin versus Placebo | HFS | double blind Follow-up duration: 3 weeks |
Warfarin versus Sudoxicam | |||
Hume, 1973 | Warfarin versus Sudoxicam | THR | single blind Follow-up duration: Discharge |
Warfarin versus unfractionated heparin | |||
Hume, 1973 | Warfarin versus UFH 5000 x3 | THR | Open Follow-up duration: Discharge |
Barber, 1977 | Warfarin versus UFH 5000 x2 | THR | Open Follow-up duration: 11–14 days |
ximelagatran versus Dalteparin | |||
METHRO I, 2002 | Melagatran 1–4 mg s.c. immediately before surgery, melagatran at 20.00 hours, then ximelagatran 6–24 mg orally b.d. for 6–9 days versus Dalteparin 5000 IU o.d., started evening before surgery for 6–9 days | adults undergoing hip or knee replacement | open Follow-up duration: 6–9 days Swedish |
METHRO II, 2002 | Melagatran 1–3 mg s.c. immediately before surgery,melagatran same day, then ximelagatran 8–24 mg orally b.d. for 7–10 days versus Dalteparin 5000 IU o.d., started evening before surgery for 7–10 days | undergoing hip or knee replacement | double-blind Follow-up duration: 7–10 days |
ximelagatran versus Enoxaparin | |||
Platinum (Colwell), 2003 | Ximelagatran 24 mg orally b.d., starting at least 12 h after surgery for 7–12 days versus Enoxaparin 30 mg s.c. b.d.,starting at least 12 h after surgery for 7–12 days | adults undergoing hip replacement | double-blind Follow-up duration: 7–12 days USA, Canada, Israel, Mexico,Argentina, South Africa |
METHRO III, 2002 | Melagatran 3 mg s.c. 4–12h after surgery, then ximelagatran24 mg orally b.d. for 7–10 days versus Enoxaparin 40 mg s.c. o.d. 12 h before surgery for 7–10 days | hip or knee replacement | double-blind Follow-up duration: 8–11 days Europe, South Africa |
Phase II (Heit), 2001 | Ximelagatran 8, 12, 18 or 24 mgorally b.d., at least 12 h after surgery for 6–12 days versus Enoxaparin 30 mg s.c. b.d.,starting at least 12 h after surgery for 6–12 days | adults (age>18 years and weight at least 40 kg) undergoing knee replacements | double-blind Follow-up duration: 6–12 days North American |
EXPRESS, 2003 | Melagatran 2 mg s.c. up to 30 min before surgery, then melagatran 3 mg at least 8 hafter surgery, then ximelagatran 24 mg orally b.d. for 8–11 days versus Enoxaparin 40 mg s.c. o.d.,starting 12 h before surgery for 8–11 days | hip or knee replacement | double-blind Follow-up duration: 8–11 days Europe |