Clinical Trials Directory

Trials / Completed

CompletedNCT00130286

Growth Hormone and/or Rosiglitazone for HIV-Associated Increased Abdominal Fat and Insulin Resistance

Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of Recombinant Human Growth Hormone and/or Rosiglitazone in the Treatment of Human Immunodeficiency Virus-Associated Visceral Adiposity and Insulin Resistance

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
77 (actual)
Sponsor
Weill Medical College of Cornell University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine if the combination of recombinant human growth hormone plus rosiglitazone (an insulin-sensitizing drug) is safe and more effective than either drug alone (or no active therapy) for the treatment of fat accumulation in people with HIV infection and insulin resistance.

Detailed description

A number of people with HIV infection who gain weight in the abdomen (sometimes called lipodystrophy) also have a high level of the sugar-controlling hormone called insulin. These people need to produce this extra insulin to help keep their blood sugar normal. This is called "insulin resistance." Studies have shown that growth hormone (also called "Serostim") can decrease abdominal fat, but it can also worsen the insulin resistance. Rosiglitazone (also called "Avandia") is used to treat insulin resistance in people who have diabetes, so we want to see if taking growth hormone and rosiglitazone together will be better for treating the fat accumulation part of lipodystrophy than either drug alone or no active therapy. The study is 24 weeks long, divided into two 12-week parts. The first part of the study is double-blind, meaning that neither participants nor the study staff will know which drugs participants are on. Participants will be assigned randomly (like flipping a coin) to one of four groups: 1. Growth hormone (one injection, daily) PLUS rosiglitazone (one tablet, twice daily). 2. Growth hormone PLUS rosiglitazone placebo ("sugar pill"). 3. Growth hormone placebo (plain water injection) PLUS rosiglitazone. 4. Growth hormone placebo PLUS rosiglitazone placebo. Everyone in the study will need to be hospitalized overnight for special tests at the beginning of the study and at week 12. The second part of the study is open-label, meaning that participants and the study staff will know which drugs participants are receiving. All volunteers will receive both active drugs: * Growth hormone (one 2 mg injection, every other day) PLUS rosiglitazone (one 4 mg tablet, twice daily).

Conditions

Interventions

TypeNameDescription
DRUGRosiglitazone4 mg tablet twice a day x 12 weeks (double-blind phase)
DRUGRecombinant human growth hormone + rosiglitazoneRecombinant human growth hormone or placebo 3 mg s.c. x 12 weeks (double-blind phase)

Timeline

Start date
2005-03-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2005-08-15
Last updated
2014-02-13
Results posted
2014-02-13

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00130286. Inclusion in this directory is not an endorsement.