Combination of amlodipine plus angiotensin receptor blocker or diuretics in high-risk hypertensive patients: a 96-week efficacy and safety study

L Ma, W Wang, Y Zhao, Y Zhang, Q Deng, M Liu… - American Journal of …, 2012 - Springer
Abstract Background and Objectives Antihypertensive therapy is effective in reducing the
risk of major adverse cardiovascular events. However, blood pressure (BP) control rate …

Effects of amlodipine plus telmisartan or amlodipine plus amiloride regimen on blood pressure control in hypertensive patients: preliminary report of Chinese …

W Wang, LY Ma, MB Liu, Q Deng… - Zhonghua Xin Xue …, 2009 - europepmc.org
Objective To evaluate the effects of amlodipine-based antihypertensive combination
regimen on blood pressure control and impact on cardiovascular events. Methods From Oct …

The combination of amlodipine and angiotensin receptor blocker or diuretics in high-risk hypertensive patients: rationale, design and baseline characteristics

W Wang, L Ma, Y Zhang, Q Deng, M Liu… - Journal of human …, 2011 - nature.com
Abstract The Chinese Hypertension Intervention Efficacy Study (CHIEF) is a multi-centre
randomized controlled clinical trial comparing the effects of amlodipine+ angiotensin II …

Efficacy and tolerability of amlodipine/valsartan combination therapy in hypertensive patients not adequately controlled on amlodipine monotherapy

H Schunkert, RD Glazer, M Wernsing… - … medical research and …, 2009 - Taylor & Francis
Objective: This study was designed to explore antihypertensive efficacy and safety of a
combination of amlodipine (CCB) and valsartan (ARB), in essential hypertensive patients …

A 48‐week study of amlodipine plus amiloride/hydrochlorothiazide vs. amlodipine plus telmisartan in the treatment of hypertension

F Lu, Y Zhao, Z Liu, H Sun, Y Zhao… - … journal of clinical …, 2012 - Wiley Online Library
Summary Background: Chinese Hypertension Intervention Efficacy (CHIEF) study is a large‐
scale randomised clinical trial across China, which compares the efficacy of two combination …

Long-term tolerability and efficacy of the combination of amlodipine/valsartan in hypertensive patients: a 54-week, open-label extension study

T Philipp, RD Glazer, Y Zhao… - Current Medical Research …, 2009 - Taylor & Francis
Objective: To evaluate the long-term tolerability and efficacy of the amlodipine/valsartan
5/320 mg once daily (od) combination in hypertensive patients. Methods: This was a 54 …

Prospective direct comparison of antihypertensive effect and safety between high-dose amlodipine or indapamide in hypertensive patients uncontrolled by standard …

K Okamura, K Shirai, N Totake, T Okuda… - Clinical and …, 2018 - Taylor & Francis
Objective: When hypertension is uncontrolled by routine treatment with an angiotensin II
receptor blocker (ARB) and the calcium channel blocker amlodipine (5 mg), the dose of …

Meta-analysis of three observational studies of amlodipine/valsartan in hypertensive patients with additional risk factors

S Eckert, SB Freytag, A Mueller, SHG Klebs - Blood pressure, 2013 - Taylor & Francis
Objectives. In this study, the effectiveness of amlodipine/valsartan single-pill combination
was assessed in hypertensive patients with diabetes, metabolic risk or overweight. Methods …

The combination of amlodipine/valsartan 5/160 mg produces less peripheral oedema than amlodipine 10 mg in hypertensive patients not adequately controlled with …

J Schrader, A Salvetti, C Calvo… - … Journal of Clinical …, 2009 - Wiley Online Library
Aims: To demonstrate the benefit of the combination amlodipine/valsartan 5/160 mg over
amlodipine 10 mg, in producing a lower incidence of peripheral oedema for a comparable …

Initial combination therapy with amlodipine/valsartan compared with monotherapy in the treatment of hypertension

T Philipp, RD Glazer, M Wernsing, J Yen - Journal of the American Society …, 2011 - Elsevier
Achieving target blood pressure (BP) is influenced by baseline BP. Post hoc analyses of a
placebo-controlled trial of amlodipine/valsartan versus monotherapies were conducted to …