The purpose of this study is to study the effect of two doses of olmesartan medoxomil and amlodipine on vascular markers in hypertensive patients with metabolic syndrome.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
60
Olmesartan medoxomil tablets low dose, taken once daily for 6 weeks
Olmesartan medoxomil tablets high dose, taken once daily for 6 weeks
Amlodipine tablets taken once daily for 6 weeks
Unnamed facility
Erlangen, Germany
To investigate the anti-inflammatory effect of Olmesartan (OM) higher dose compared to Olmesartan (OM) lower dose and amlodipine (AML) on the change in levels of the inflammatory marker hs-CRP
Time frame: 6 weeks for each treatment
To evaluate the additional antihypertensive efficacy in blood pressure (BP) lowering, assessed by conventional BP measurement and 24-h ambulatory BP measurement (24-h ABPM)
Time frame: 6 weeks for each treatment
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