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Completed

NCT Number: NCT00140244

Randomized, Placebo-Controlled Study of Leptin for the Treatment of HIV Lipodystrophy and Metabolic Syndrome

The purpose of this study is to examine whether replacing leptin to normal levels can reverse the changes in fat distribution, lipid profile, and other metabolic problems associated with highly active antiretroviral therapy (HAART)-induced lipodystrophy and metabolic syndrome in HIV patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Beth Israel Deaconess Medical Center

Boston, Massachusetts, 02215, United States

About this study

Exposure to HIV medications has been associated with metabolic changes including generalized fat depletion (lipoatrophy), high triglyceride levels, and in some patients, high sugar levels or diabetes. This syndrome is associated with a deficiency of leptin, a hormone produced by fat cells. Recent studies involving leptin administration to patients with congenital lipoatrophy have shown dramatic improvements in metabolic parameters such as insulin resistance and hyperlipidemia. Leptin administration to patients with HAART-induced lipoatrophy may also lead to significant improvements in the metabolic abnormalities found in these HIV+ patients. The aims of this study are to examine the effect of leptin administration on insulin resistance and other parameters of the metabolic syndrome in HIV patients with HAART-induced lipoatrophy.

Comparison: Leptin-treated group to placebo-treated group

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 18 years old
  • Documented HIV infection
  • Exposed to at least 6 months of cumulative highly active antiretroviral medications for HIV
  • Developed fat depletion after starting HIV medications
  • Low leptin level in the blood
  • Fasting triglyceride level > 300 mg/dl

Exclusion criteria

  • Active infectious diseases, except HIV
  • Diabetes prior to starting HIV medications
  • Alcohol or drug abuse
  • Triglyceride level > 1000 mg/dl
  • Significant kidney, liver, or thyroid dysfunction
  • Cancer or lymphoma
  • Pregnancy or planning to become pregnant during the study

Treatment and study plan

r-metHuLeptin

Drug

Placebo

Drug

Primary outcomes

  1. Serum Lipid Levels

    Time frame: At the end of each two month intervention

Secondary outcomes

  1. Insulin Resistance (as Assessed by HOMA-IR)

    Time frame: At the end of each two month intervention

  2. Glycemia (as Assessed by Fasting Glucose)

    Time frame: At the end of each two month intervention

  3. Low Density Lipoprotein (LDL) Cholesterol Levels

    Time frame: At the end of each two month intervention

  4. Free Fatty Acid (FFA) Levels

    Time frame: At the end of each two month intervention

  5. Blood Pressure

    Time frame: At the end of each two month intervention

    percent change in mean blood pressure

  6. Fibrinogen

    Time frame: At the end of each two month intervention

    Fibrinogen

  7. Insulin Levels

    Time frame: At the end of each two month intervention

  8. Lean Body Mass

    Time frame: At the end of each two month intervention

    lean body mass

  9. Viral Load

    Time frame: At the end of each two month intervention

  10. CD4+ Lymphocytes

    Time frame: At the end of each two month intervention

  11. Interleukin-6 (IL-6) Levels

    Time frame: At the end of each two month intervention

  12. Hepatic Fat Content

    Time frame: At the end of each two month intervention

Sponsors and collaborators

Lead sponsor

Beth Israel Deaconess Medical Center

Other

Collaborators

  • Amgen
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Official study title

Role of Leptin in Highly Active Antiretroviral Therapy (HAART)-Induced Lipodystrophy and Metabolic Syndrome in HAART-Treated HIV Patients

Important dates

Study start
2001
Primary completion
2011
Study completion
2011
First posted
Sep 1, 2005
Registry last updated
May 11, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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