The purpose of this study is to evaluate of efficacy and safety of amlodipine plus losartan and amlodipine alone in patients with essential hypertension inadequately controlled on amlodipine monotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
185
amlodipine/losartan 5/50mg q.d.
amlodipine 5mg q.d.
13 sites in Korea
Seoul, Busan, Etc., South Korea
Change from baseline in mean sitting diastolic blood pressure
Time frame: Week 8
Change from baseline in mean sitting diastolic blood pressure
Time frame: Week 4
Change from baseline in mean sitting systolic blood pressure
Time frame: Week 4, 8
Responder rate
Time frame: Week 4, 8
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