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Lipodystrophy clinical trials

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NCT ID: NCT00608023 Completed - HIV Infections Clinical Trials

TH9507 Extension Study in Patients With HIV-Associated Lipodystrophy

Start date: August 2007
Phase: Phase 3
Study type: Interventional

Assessing the Efficacy and Long-Term Safety of a 2 mg dose of TH9507, a Growth Hormone-Releasing Factor Analog, in HIV Subjects with Excess Abdominal Fat Accumulation

NCT ID: NCT00585715 Completed - Clinical trials for Localized Lipodystrophy

Evaluation of the Candela 1064nm:Nd:YAG Laser for Skin Tightening

IH062905
Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of this research study is to evaluate effectiveness of a non-ablative (does not remove skin) treatment for cellulite (dimpled fat) in conjunction with skin tightening using the Candela GentleYAG laser.

NCT ID: NCT00461552 Completed - HIV Infections Clinical Trials

Therapeutic Approaches to HAART-Induced Lipodystrophy

Start date: January 2003
Phase: Phase 2
Study type: Interventional

To determine the efficacy and safety of 4 therapeutic interventions on HAART-Induced lipodystrophy. The interventions are: 1) Dietary - the effect of a high carbohydrate vs.a high cis-monounsaturated fatty acid diet. 2) The effect of aerobic exercise with dietary advice. 3) The effect of Omega-3 Fish Oil Capsules. 4) The effect of leptin therapy. These interventions are aimed at improving the metabolic complications of HAART therapy such as elevated lipids, and insulin resistance or diabetes.

NCT ID: NCT00457938 Completed - Diabetes Clinical Trials

Novel Therapies for Metabolic Complications of Lipodystrophies

Start date: April 2006
Phase: N/A
Study type: Interventional

Lipodystrophies represent a therapeutic challenge with regards to the management of the diabetes, insulin resistance, hypertriglyceridemia and fatty liver which frequently present in conjunction with significant adipose tissue loss. The purpose of the study and it's four subprojects is to examine the safety and efficacy of various novel interventions designed to improve or resolve the fatty liver, hypertriglyceridemia, and insulin resistance or diabetes that is seen in these patients.

NCT ID: NCT00457665 Completed - HIV Infections Clinical Trials

Mechanisms of Lipodystrophy in HIV-Infected Pateints

Start date: February 2002
Phase: Phase 4
Study type: Interventional

The metabolic and molecular basis of lipodystrophy syndrome in HIV-infected patients is not known. Whether besides protease inhibitors, other antiretroviral drugs, HIV infection and reduction in viral load contribute to the development of lipodystrophy syndrome is not clear. The project therefore has the following aims: 1) to characterize metabolic abnormalities and changes in body fat distribution, 2) to develop objective criteria for defining the syndrome and to ascertain prognostic indicators and 3) to elucidate the molecular basis of the lipodystrophy syndrome in HIV-infected patients.

NCT ID: NCT00457639 Completed - Hepatic Steatosis Clinical Trials

Cholic Acid for Hepatic Steatosis in Lipodystrophy

Start date: April 2006
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of cholic acid therapy in treating lipodystrophy patients with hepatic steatosis. This is a randomized, double-blind, placebo-controlled cross-over study.

NCT ID: NCT00383734 Completed - Clinical trials for HIV-Associated Lipodystrophy Syndrome

Safety and Efficacy of Intradermal Injections of Newfill Versus Eutrophill in the Treatment of Facial Lipoatrophy in HIV-infected Patients ANRS 132 SMILE

Start date: December 2006
Phase: Phase 3
Study type: Interventional

Treatment of facial lipoatrophy with dermal injections polylactic acid (Newfill TM) is a safe procedure and has been now widely used with a good efficacy. However, this therapy is not effective in all treated patients and the benefit of the injections may decrease with time necessitating re-injections several months after the first sets of injections. In this study we would like to compare the efficacy and safety of Eutrophill(polyacrylamid gel), a resorbable filler compound versus Newfill in a comparative, randomised, multicenter trial. Primary endpoint will be the self-perception by the patient with a visual analogue scale (VAS index). Secondary endpoints are a quality of life questionnaire (MOS-HIV), the a-NBC questionnaire (perception by the patient and by the doctor of the severity of the lipoatrophy), the measure of the dermal thickness and cheek skin fold as assessed by the Skinfold Caliper, the ordering of digital photographs and the evaluation of the dermal thickness by CT scan.

NCT ID: NCT00367744 Completed - HIV Infections Clinical Trials

Rosiglitazone Effect on Mitochondria and Lipoatrophy

Start date: July 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the effect of rosiglitazone on limb fat and mitochondrial indices in HIV-1-infected subjects receiving stable antiretroviral therapy that does not contain stavudine (d4T) or zidovudine (AZT).

NCT ID: NCT00362440 Completed - HIV Lipodystrophy Clinical Trials

Combination of Insulin Sensitizer and Leptin as Treatment for the HAART -Induced Metabolic Syndrome

Start date: August 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether patients with HIV lipodystrophy (fat wasting) benefit from taking the combination of two drugs, one insulin sensitizer (either metformin or pioglitazone, both diabetes drugs) and leptin (a natural hormone produced by your fat cells). Our hope is that they will improve sugar and fat metabolism and positively affect the body fat changes you have noticed while taking HAART.

NCT ID: NCT00360932 Completed - Facial Lipoatrophy Clinical Trials

Facial Lipoatrophy Correction Experience With SCULPTRA ("FACES" Study)

FACES
Start date: October 2005
Phase:
Study type: Observational

5 year, open-label study to evaluate safety of SCULPTRA on the signs of lipoatrophy of the face in at least 100 evaluable subjects with human immunodeficiency virus.