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Completed Not applicable Interventional

Effects of Treatment Changes on Fat Wasting in the Arms and Legs of HIV Patients

ClinicalTrials.gov ID: NCT00028314

Public ClinicalTrials.gov record NCT00028314. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 5:16 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Restrictively Randomized, Open-Label, Controlled, Pilot Study of the Effect of a Thymidine Analogue Substitution or Change to a Nucleoside-Sparing Regimen on Peripheral Fat Wasting

Study identification

NCT ID
NCT00028314
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
150 participants

Conditions and interventions

Interventions

  • Abacavir sulfate Drug
  • Atazanavir/Ritonavir Drug
  • Lopinavir/Ritonavir Drug
  • Nevirapine Drug

Drug

Eligibility (public fields only)

Age range
13 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2002
Primary completion
Not listed
Completion
Feb 28, 2005
Last update posted
Jul 28, 2013

2002 – 2005

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
UCLA CARE Center CRS Los Angeles California 90095
Harbor-UCLA Med. Ctr. CRS Torrance California 90502-2052
University of Colorado Hospital CRS Aurora Colorado 80262
Univ. of Hawaii at Manoa, Leahi Hosp. Honolulu Hawaii 96816
Northwestern University CRS Chicago Illinois 60611
Rush Univ. Med. Ctr. ACTG CRS Chicago Illinois 60612
Cook County Hosp. CORE Ctr. Chicago Illinois
Indiana Univ. School of Medicine, Infectious Disease Research Clinic Indianapolis Indiana
Indiana Univ. School of Medicine, Wishard Memorial Indianapolis Indiana
Methodist Hosp. of Indiana Indianapolis Indiana
Beth Israel Deaconess Med. Ctr., ACTG CRS Boston Massachusetts 02215
SSTAR, Family Healthcare Ctr. Fall River Massachusetts
University of Minnesota, ACTU Minneapolis Minnesota 55455-0392
St. Louis ConnectCare, Infectious Diseases Clinic St Louis Missouri 63108
Washington U CRS St Louis Missouri 63108
Beth Israel Med. Ctr., ACTU New York New York 10003
NY Univ. HIV/AIDS CRS New York New York 10016
Univ. of Cincinnati CRS Cincinnati Ohio 45267-0405
MetroHealth CRS Cleveland Ohio 44109-1998
The Ohio State University Medical Center Columbus Ohio 432101228
Hosp. of the Univ. of Pennsylvania CRS Philadelphia Pennsylvania 19104
The Miriam Hosp. ACTG CRS Providence Rhode Island 02906
Rhode Island Hosp. Providence Rhode Island
Vanderbilt Therapeutics CRS Nashville Tennessee 37203
Univ. of Texas Medical Branch, ACTU Galveston Texas 775550435

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00028314, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 28, 2013 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00028314 live on ClinicalTrials.gov.

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