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A Study to Determine How and Why HIV-Infected Subjects on Anti-viral Treatment Develop Lipodystrophy

The Study of Mechanisms of Lipodystrophy in HIV-Infected Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00006190
Enrollment
Unknown
Registered
2000-08-28
Start date
2000-11-30
Completion date
2001-11-30
Last updated
2010-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections, Lipodystrophy

Keywords

Lipoproteins, Insulin resistance, Adipose tissue

Brief summary

HIV infection is a major global health problem. Survival and quality of life for HIV subjects has tremendously improved with the advent of a class of antivirals called protease inhibitors and the utilization of highly active combination therapy. However, such therapy has been associated with a syndrome called lipodystrophy. This lipodystrophy syndrome causes body shape changes; typically thinning and loss of fat from the arms, legs and face, with increased fat appearing in the abdomen and neck. There are also metabolic changes which occur, and subjects can develop increased triglycerides, increased cholesterol and an increased risk for diabetes as indicated by increasing insulin resistance. This study will take HIV positive subjects who have not yet started antiviral medications (treatment naive)and randomly assign them to one of two treatment arms. These treatment arms will be: Sustiva/Zerit/Epivir vs. Viracept/Zerit/Epivir The subjects will be treated and followed for two years and have extensive metabolic testing, skinfold thickness measurements, MRI scans and other measures to determine if and how they are experiencing changes in metabolism or body shape and to discover the mechanism of why this occurs. Understanding the mechanism should allow researchers to design interventions for subjects who have lipodystrophy and strategies to prevent lipodystrophy from occurring to subjects treated with antivirals in the future.

Interventions

DRUGNelfinavir mesylate
DRUGStavudine
DRUGLamivudine
DRUGEfavirenz

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Lead SponsorNIH

Study design

Primary purpose
DIAGNOSTIC
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* CD4 count \> 200 cells/mm * HIV RNA (viral load) \<= 100,000 copies/ml * No previous antiviral therapy

Exclusion criteria

* AIDS or opportunistic infections * Active intravenous drug users * Use of: corticosteroids, androgens, lipid-lowering drugs, anti-fungal medications, oxandrolone, megace, dehydroepiandrosterone. * Subjects with diabetes mellitus * Subjects who consume \> 2 alcoholic drinks per day * Pregnant women, premenopausal women unless adequate birth control is in use. * Acute or chronic liver diseases, liver enzymes elevations \> 2.5 times the upper limit of normal. * Anemia, an Hct \< 35% for men, or \< 32% for women. * Abnormal thyroid function tests.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026