The purpose of this study is to evaluate the antihypertensive effect of AGSCT101 tablet in patient with stage 1 to 2 essential hypertension.
This study is 2,8 weeks, multi-center, randomized, double-blind, active clinical trial to evaluate the efficacy and safety of AGSCT101 versus Carvedilol in patient with stage 1 to 2 essential hypertension.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
260
Tablet, q.d.
Tablet, q.d.
The Catholic University of Korea-St. Mary's Hospital
Seoul, South Korea
RECRUITINGChange from baseline in diastolic blood pressure (DBP)
Time frame: 8 weeks
Change from baseline in diastolic blood pressure (DBP)
Time frame: 2 weeks
Change from baseline in systolic blood pressure (SBP)
Time frame: 2, 8 weeks
Proportion of patients who reach overall blood pressure control (defined as BP <140/90)
Time frame: 8 weeks
Incidence of adverse effects
Time frame: 8 weeks
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