A double blind study to examine the safety and efficacy of different dosages of lercanidipine in normal weight and obese patients with hypertension
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
180
change from baseline of systolic blood pressure (BPs) after 4 weeks of treatment
Blood pressure, response rate, normalization rate, pulse rate, lipid profile, safety and tolerability. Measures after 4, 8, 12 weeks.
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