Trials / Completed
CompletedNCT01395602
Effect of Cabergoline on Weight and Glucose Tolerance
Randomized Controlled Pilot Study of the Effect of Cabergoline on Body Weight and Glucose Tolerance in Healthy Obese Adults
- Status
- Completed
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Columbia University · Academic / Other
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
The aim of this study is to determine the efficacy of cabergoline, a long-acting dopamine receptor agonist, on body weight and blood glucose in healthy obese adults. This is a randomized double-blind placebo controlled study. Twenty subjects each will be randomly assigned either placebo or cabergoline for 16 weeks. The effect of treatment on body weight and blood glucose and insulin levels will be compared in the treatment versus the placebo arm.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Cabergoline | cabergoline 0.5 mg twice weekly |
| OTHER | placebo | 1 pill twice weekly |
Timeline
- Start date
- 2002-04-01
- Primary completion
- 2003-09-01
- Completion
- 2011-07-01
- First posted
- 2011-07-15
- Last updated
- 2015-10-14
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01395602. Inclusion in this directory is not an endorsement.