ARBs versus control | |||
Suzuki, 2008 | ARBs (valsartan, candesartan, and losartan) versus no ARBs | patients with diabetes and chronic kidney disease on dialysis | open |
candesartan versus amlodipine | |||
CASE-J, 2008 | candesartan-based regimen versus amlodipine-based regimen | high-risk Japanese hypertensive patients | open (blinded assessment) Follow-up duration: 3.2 years Japan |
candesartan versus control | |||
Takahashi, 2006 | candesartan versus control | patients on chronic haemodialysis in stable condition and with no clinical evidence of cardiac disorders | open Follow-up duration: 19.4 months |
candesartan versus conventional treatment | |||
E-COST, 2005 | candesartan, 2 to 12 mg daily versus conventional antihypertensive drugs other than angiotensin converting enzyme inhibitors or ARBs | Japanese essential hypertensive subjects (sitting blood pressure 140-180/90-110 mmHg) aged 35-79 years | single-blind Japan |
E-COST-R, 2005 | candesartan versus conventional treatment | hypertensive subjects 60 to 75 years old with non-diabetic chronic renal insufficiency | open |
HIJ-CREATE, 2009 | angiotensin II receptor blocker-based therapy versus non-angiotensin II receptor blocker-based therapy | patients with angiographically documented coronary artery disease and hypertension | open Follow-up duration: 4.2 y (median) Japan |
candesartan versus hydrochlorothiazide | |||
ALPINE, 2003 | candesartan versus hydrochlorothiazide | newly detected hypertensives | double-blind Follow-up duration: 1 year Sweden |
candesartan versus placebo | |||
TROPHY, 2006 NCT00227318 | candesartan during 2y followed by 2y
of placebo versus placebo | subjects with repeated measurements of systolic pressure of 130 to 139 mm Hg and diastolic pressure of 89 mm Hg or lower, or systolic pressure of 139 mm Hg or lower and diastolic pressure of 85 to 89 mm Hg | double-blind Follow-up duration: 4y USA |
SCOPE, 2003 | candesartan, 8–16 mg once daily (target 160/90) versus placebo | patients aged 70–89 years, with systolic blood pressure 160– 179 mmHg, and/or diastolic blood pressure 90–99 mmHg, and a Mini Mental State Examination (MMSE) test score > 24 | double-blind Follow-up duration: 3.7 y (mean) 15 countries |
irbesartan versus amlodipine | |||
IDNT (irbesartan vs amlodipine), 2001 | Irbesartan 300mg/d (with a target of 135/85) versus amlodipine 10mg/d (with a target of 135/85) | hypertensive patients with nephropathy due to type 2 diabetes | double-blind Follow-up duration: 2·6y worldwide |
irbesartan versus placebo | |||
IDNT (irbesartan vs pbo), 2001 | Irbesartan 300mg/d (target 135/85) versus placebo | hypertensive patients with nephropathy due to type 2 diabetes | double-blind Follow-up duration: 2.6 y worldwide |
IRMA 2, 2001 | irbesartan 150 mg daily or 300 mg daily versus placebo | hypertensive patients with type 2 diabetes and microalbuminuria | double-blind Follow-up duration: 2 years multinational |
LCZ696 versus placebo | |||
Ruilope, 2010 | LCZ696 for 8 weeks versus placebo | patients with mild to moderate hypertension | double blind Follow-up duration: 8 weeks 18 countries |
losartan versus atenolol | |||
LIFE, 2002 | losartan versus atenolol | patients aged 55–80 years, with previously treated or untreated hypertension (sitting blood pressure 160–200/95–115 mm Hg) and ECG signs of LVH. | Double blind Follow-up duration: 4.8 y (mean) USA, Europe |
losartan versus placebo | |||
RENAAL, 2001 | lLosartan 50 to 100 mg once daily versus placebo | patients with type 2 diabetes and nephropathy | double-blind Follow-up duration: 3.4 years |
olmesartan versus placebo | |||
ROADMAP, 2010 NCT00185159 | olmesartan at 40 mg/day versus placebo | patients with diabetes and at least one additional cardiovascular risk factor, but no evidence of renal dysfunction | double-blind Follow-up duration: 3.2 y Europe (19 countries) |
ORIENT, NCT00141453 | olmesartan versus placebo | patients with diabetic Nephropathy and overt proteinuria secondary to type 2 diabetes mellitus | double-blind Japan, Hong Kong |
olmesartan 40 mg versus olmesartan 20 mg plus a calcium-channel blocker | |||
OSCAR, 2011 NCT00134160 | high-dose olmesartan 40 mg per day versus 20-mg/day olmesartan comined with standard dose of amlodipine or azelnidipine | high-risk elderly Japanese hypertension patients | Japan |
telmisartan versus enalapril | |||
DETAIL, 2004 | telmisartan 80 mg daily versus enalapril 20 mg daily | subjects with type 2 diabetes and early nephropathy | double-blind Follow-up duration: 5 year |
telmisartan versus placebo | |||
TRANSCEND, 2008 NCT00153101 | telmisartan 80 mg/day versus placebo | high-risk patients intolerant to angiotensin-converting enzyme inhibitors | double blind Follow-up duration: median 56 months (IQR 51-64) 40 countries |
PROPHESS, 2008 NCT00153062 | telmisartan 80 mg daily versus placebo | patients who recently had an ischemic stroke | double blind Follow-up duration: 2.5 y 35 countries |
telmisartan versus ramipril | |||
ONTARGET (telmisartan alone), 2008 NCT00153101 | telmisartan 80mg daily versus ramipril 10 mg daily | patients patients with coronary, peripheral, or cerebrovascular disease or diabetes with end-organ damage | double blind Follow-up duration: 4.7y 40 countries |
telmisartan + ramipril versus ramipril | |||
ONTARGET (association vs ramipril), 2008 NCT00153101 | telmisartan 80mg + ramipril 10mg daily versus ramipril 10 mg daily | patients patients with coronary, peripheral, or cerebrovascular disease or diabetes with end-organ damage | double blind Follow-up duration: 4.7y 40 countries |
telmisartan + ramipril versus telmisartan | |||
ONTARGET (association vs telmisartan), 2008 NCT00153101 | telmisartan 80mg + ramipril 10mg daily
versus telmisartan 80 mg daily | patients patients with coronary, peripheral, or cerebrovascular disease or diabetes with end-organ damage | double blind Follow-up duration: 4.7y 40 countries |
valsartan versus amlodipine | |||
VALUE, 2004 NCT00129233 | valsartan based regimen versus amlodipine based regimen | patients, aged 50 years or older with treated or untreated hypertension and high risk of cardiac events | Double blind Follow-up duration: 4.2 y (mean) 31 countries |