Obesity Clinical Trial
Official title:
Double Blind Study of Irbesartan vs. Amlodipine in Obese Hypertensive Subjects- The OBI Study
Objective:
1. To study the effectiveness of irbesartan 300mg and amlodipine 10 mg in 24h ambulatory
blood pressure values in obese subjects
2. To study the drug specific effect in arterial stiffness
3. To study possible drug mechanisms in obesity (reduction of central adiposity and
changing the ratio of leptin to adiponectin)
Study Objectives
1. Primary:
- Reduction of 24h BP in obese hypertensives
- Reduction in arterial stiffness
2. Secondary
- Drug specific effect on new onset of diabetes
- Drug specific effect on reduction in central fat deposition and the leptin to
adiponectin ratio
Study design
Study drugs: Irbesartan 300mg vs. amlodipine 10mg
Tx duration and follow-up: 12 months
Collected data:
- 24h SBP and DBP in time 0, 1, 12.
- Pulse wave velocity in time 0,1,12.
- Central obesity (total, visceral, abdominal fat) in time 0,1,12.
- Leptin/adiponectin in time 0,1,12.
- BMI, waist/hip ratio in time 0,1, 12.
- Glu, HbA1c, insulin in time 0, 1,12.
- K, Na, Cr, BUN, Chol, Tg, HDL, LDL,ALT, AST in time 0, 1,12. Number of patients: The
reduction in mean SBP expected to be 15 mmHg. Previous studies from our group reported
an 14mmHg SD for mean SBP. The sample size required at the two sided 5% significance
level and 80% power is 40 patients (Lehr's formula)
Number of centers: 1
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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