apixaban versus enoxaparin | |||
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 |
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 placebo | |||
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 |
certoparin versus UFH | |||
CERTIFY, 2010 | versus | ||
dalteparin versus placebo | |||
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 |
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 |
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 |
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 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 |
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 |
fondaparinux versus enoxaparin | |||
BRiEF, NCT00521885 | fondaparinux 2.5mg qd versus enoxaparin 40mg qd | acute medically ill, non-surgical patients | Germany |
fondaparinux versus placebo | |||
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 |
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 placebo | |||
Bergmann, 1996 | nadroparin 7500 u anti-Xa once daily versus placebo | hospitalized medical | Follow-up duration: up to 21 |
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 |
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 |
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 |
ticlopidine versus placebo | |||
McKenna-II , 1983 | Ticlopidine versus placebo | high risk (post CVA) medical patients | double-blind |
UFH versus control | |||
Blech, 1981 | Unfractionated heparin, 5000 U trice daily, until mobilized versus control | Heart failure, chest infection | open Follow-up duration: <=14 days |
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 |
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 |
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