This study aims to evaluate the efficacy and safety of the coadministration of valsartan (Diovan®) 160mg and rosuvastatin (Crestor®) 20mg in comparison to each component administered alone in patients with hypertension and hyperlipidemia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
168
Yonsei University Health System Severance Hospital
Seoul, South Korea
sitDBP Changes at Week 8 From Baseline
sitDBP changes of the valsartan 160mg and valsartan placebo groups at Week 8 from baseline
Time frame: 8 weeks
LDL-C Percentage Changes at Week 8 From Baseline
LDL-C percentage changes of the rosuvastatin 20mg and rosuvastatin placebo groups at Week 8 from baseline
Time frame: 8 weeks
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