|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsored by: |
National Center for Research Resources (NCRR) |
|---|---|
| Information provided by: | National Center for Research Resources (NCRR) |
| ClinicalTrials.gov Identifier: | NCT00006493 |
Purpose
The purpose of this research is to study the effects of rosiglitazone, a drug usually taken for Type II diabetes, on HIV-associated hyperlipidemia.
HIV-associated lipodystrophy is a medical condition characterized by gradual changes in the distribution of body fat. The body fat located in the extremities and face disappears while body fat around the abdomen and upper back increases. Certain biochemical changes occur in association with these changes in fat distribution. Lipid levels particularly serum triglycerides are increased. HDL, the "good cholesterol" is decreased. Higher than normal level of insulin or insulin resistance is also found in this condition. This latter condition is one of the hallmarks of Type II diabetes.
The protease inhibitors, a class of HIV medications, are associated with the occurrence of HIV-associated lipodystrophy. It has been suggested that a biochemical pathway known as the peripheral peroxisomal activating receptor (PPAR) gamma system is blocked leading to the onset of this condition.
Rosiglitazone is a new drug approved by the FDA in 1999 for the treatment of type II diabetes. It lowers blood sugar by improving insulin resistance, which as mentioned before, is the hallmark of Type II diabetes. It has also been noted to improve blood lipid levels. Rosiglitazone works by stimulating the PPAR gamma system. It is hoped that this drug can turn on the PPAR system and reverse the HIV-associated lipodystrophy syndrome.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections Hyperlipidemia |
Drug: Rosiglitazone |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Open Label |
Eligibility| Ages Eligible for Study: | 18 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | NCRR-M01RR00096-1006, M01RR00096 |
| Study First Received: | November 14, 2000 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00006493 History of Changes |
| Health Authority: | United States: Federal Government |
|
HIV-associated hyperlipidemia |
|
Sexually Transmitted Diseases, Viral Hyperlipidemias Metabolic Diseases Acquired Immunodeficiency Syndrome Immunologic Deficiency Syndromes Virus Diseases Hypoglycemic Agents |
HIV Infections Sexually Transmitted Diseases Retroviridae Infections Metabolic Disorder Rosiglitazone Dyslipidemias Lipid Metabolism Disorders |
|
RNA Virus Infections Sexually Transmitted Diseases, Viral Metabolic Diseases Hyperlipidemias Slow Virus Diseases Immune System Diseases Physiological Effects of Drugs Acquired Immunodeficiency Syndrome Infection Pharmacologic Actions |
Immunologic Deficiency Syndromes Virus Diseases Hypoglycemic Agents HIV Infections Sexually Transmitted Diseases Lentivirus Infections Rosiglitazone Retroviridae Infections Dyslipidemias Lipid Metabolism Disorders |