Obesity Clinical Trial
Official title:
A Randomized, Double-Bind, Placebo-Controlled, Parallel-Group, Fixed-Dose, Multicenter Study to Assess Efficacy and Safety of Rimonabant 20 mg Versus Placebo on Weight Loss and Frequency of Binge Episodes in Obese Patients With Food Craving
The primary objective is to assess the effect of rimonabant compared to placebo on weight
loss over a period of 6 months when prescribed with a mild hypocaloric diet in obese
patients with binge eating disorder.
The secondary objectives are:
- to assess the effect of rimonabant on the number of binge episodes per week, to assess
the effect of rimonabant on eating behavior using the Binge Eating Scale (BES) and
Three Factor Eating Questionnaire (TFEQ),
- to evaluate the safety and tolerability of rimonabant over a period of 6 months.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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