Diabetes Mellitus, Type 2 Clinical Trial
Official title:
A Randomized, Double Blind, Placebo Controlled Study Evaluating the Glycemic Effect of Rimonabant Added to Metformin in Patients With Type 2 Diabetes Insufficiently Controlled With Metformin Monotherapy
The primary objective of the study is to determine the effect of rimonabant 20 mg daily when
added to ongoing metformin therapy on glycemic control (HbA1c) over a 36 week period in
patients with type 2 diabetes.
Secondary objectives include evaluation of other markers of glycemic control, lipid profile,
body weight, and abdominal obesity. Also, the trial will study the safety of rimonabant when
added to metformin over a period of 47 weeks.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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