The purpose of this study is to evaluate the efficacy of different fixed-dose combination of Viena II in treatment of hypertension and dyslipidemia.
* Fase II, national, multicenter, randomized, double-blind. * Maximal duration: 8 weeks; * 04 visits; * Safety and efficacy evaluation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Reduction of systemic blood pressure measured between the first visit and last visit
Time frame: 8 weeks
Percentage of reduction of LDL-c between the first visit and the last visit.
Time frame: 8 weeks
Incidence and severity of adverse events recorded during the study
Time frame: 8 weeks
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