Related trials
Ruilope, 2010 - LCZ696 vs
KYOTO HEART Study, 2009 - valsartan vs non ARB strategy
Schmieder (vs HCTZ), 2009 - aliskiren vs hydrochlorothiazide
ALLAY, 2009 - aliskiren vs losartan
AVOID, 2008 - aliskiren vs placebo
HYVET, 2008 - indapamide vs placebo
ACCOMPLISH, 2008 - amlodipine plus benazepril vs hydrochlorothiazide plus benazepril
Andersen, 2008 - aliskiren vs ramipril
PROPHESS, 2008 - telmisartan vs placebo
ASCOT-BPLA, 2005 - amlodipine vs atenolol
ASCOT-BPLA, 2005 - atenolol vs amlodipine
VALUE, 2004 - valsartan vs amlodipine
SHELL, 2003 - lacidipine vs chlorthalidone
ANBP2, 2003 - enalapril vs diuretics
CONVINCE, 2003 - Atenolol or hydrochlorothiazide vs verapamil
SCOPE, 2003 - candesartan vs placebo
INVEST (Pepine), 2003 - verapamil vs atenolol
INVEST, 2003 - atenolol vs verapamil
CONVINCE, 2003 - verapamil vs diuretic or beta-blocker
ELSA, 2002 - atenolol vs lacidipine
LIFE, 2002 - losartan vs atenolol
ELSA, 2002 - lacidipine vs atenolol
LIFE, 2002 - atenolol vs Losartan
JMIC-B, 2002 - various ACEI vs nifedipine
ALLHAT (vs chlorthalidone), 2002 - lisinopril vs diuretics
See also:
All hypertension clinical trials
All clinical trials of anti hypertensive agent
All clinical trials of amlodipine
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AASK (vs ramipril) study, 2002
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Treatments
Studied treatment |
Amlodipine 5-10 mg/d
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Control treatment |
ramipril 2.5-10 mg/d
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Remarks |
compare the effects of 2 levels of blood pressure (BP) control and 3 antihypertensive drug classe
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Patients
Patients |
African Americans aged 18 to 70 years with hypertensive renal disease (GFR, 20-65 mL/min per 1.73m2)
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Inclusion criteria |
African Americans; hypertension;
aged 18
to 70 years; glomerular filtration
rate (GFR) between 20 and 65 mL/min
per 1.73 m2; no other identified
causes of renal insufficiency |
Baseline characteristics |
Inclusion SBP |
none |
Inclusion DBP |
>=95 mmHG |
baseline BP |
150/96 |
Female (%) |
39% |
Age |
54.5y |
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Method and design
Randomized effectives |
217 / 436 (studied vs. control) |
Design |
Factorial plan |
Blinding |
Double blind |
Follow-up duration |
3�0 |
Number of centre |
21 |
Geographic area |
US |
Primary endpoint |
rate of change in GFR (GFR slope) |
Remarks |
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Remarks / Comments
Results
Endpoint
Studied treat. n/N
Control treat. n/N
Graph
RR [95% CI]
All cause death
13 / 217
29 / 436
0,90 [0,48;1,70]
0
2
1.0
Relative risks
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Endpoint |
Events (%) |
Relative Risk |
95% CI |
Endpoint definition in the trial |
Ref |
Studied treat. |
Control treat. |
All cause death
|
13 / 217 (6,0%) |
29 / 436 (6,7%) |
0,90 |
[0,48;1,70] |
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The primary endpoint (if exists) appears in blod characters
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Reference(s) used for data extraction:
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Endpoint |
studied treat. |
control treat. |
mean diff |
Absolute risk reduction
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Endpoint |
Events rate |
Absolute risk reduction (ARR) |
Studied treat. |
Control treat. |
All cause death |
5,99% |
6,65% |
-6,6‰
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Reference(s)
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Wright JT Jr, Bakris G, Greene T, Agodoa LY, Appel LJ, Charleston J, Cheek D, Douglas-Baltimore JG, Gassman J, Glassock R, Hebert L, Jamerson K, Lewis J, Phillips RA, Toto RD, Middleton JP, Rostand SG.
Effect of blood pressure lowering and antihypertensive drug class on progression of hypertensive kidney disease: results from the AASK trial..
JAMA 2002;288:2421-31
Pubmed
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Hubmed
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