drugset / Trial / NCT01184560

Assess the Additional Weight Loss Effect of Orlistat Used in Combination With Sibutramine

NCT01184560

Completed 174 enrolled Gachon University Gil Medical Center
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study, conducted academic Pilot research purposes, this is not clear as to permit. when orlistat to sibutramine merge if there are additional effects of BMI and group, which has an attribute that is greater for the combined effect is to analyze. * Study phase: Investigator-initiated clinical study (Pilot study) * Method of blinding: Double-blind * Control: Placebo-controlled * Assignment method: Randomization (Sibutramine monotherapy group: Orlistat and Sibutramine combination group = 1 : 1) * Studied disease: Obesity * Study population: Subjects eligible for inclusion/exclusion criteria * Dosing period: Total 18 weeks Run-in period (2 weeks), dosing period (12 weeks) and post-dosing observation period (4 weeks)

Timeline

Start
2010-02
Primary completion
2010-07
Completion
2010-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Orlistat Small molecule 120 mg
Background Sibutramine Small molecule 10 mg

Indications