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Completed Phase 1 Interventional

A Study to Evaluate the Effect of Nandrolone Decanoate in Women With HIV-Associated Weight Loss

ClinicalTrials.gov ID: NCT00000854

Public ClinicalTrials.gov record NCT00000854. 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, 10:01 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 Randomized, Double-Blind, Placebo-Controlled, Phase I/II Trial of Nandrolone Decanoate in Women With HIV-Associated Weight Loss

Study identification

NCT ID
NCT00000854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
38 participants

Conditions and interventions

Interventions

  • Nandrolone decanoate Drug

Drug

Eligibility (public fields only)

Age range
13 Years and older
Sex
Female
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
Not listed
Primary completion
Not listed
Completion
Apr 30, 2003
Last update posted
Oct 28, 2021

Ends 2003

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
USC CRS Los Angeles California 90033
UCLA CARE Center CRS Los Angeles California 90035
Ucsd, Avrc Crs San Diego California 92103
Ucsf Aids Crs San Francisco California 94110
University of Colorado Hospital CRS Aurora Colorado 80045
Howard University Hosp., Div. of Infectious Diseases, ACTU Washington D.C. District of Columbia 20060
Queens Med. Ctr. Honolulu Hawaii 96813
Univ. of Hawaii at Manoa, Leahi Hosp. Honolulu Hawaii 96816
Northwestern University CRS Chicago Illinois 60611
Tulane Med. Ctr. - Charity Hosp. of New Orleans, ACTU New Orleans Louisiana 70112
Johns Hopkins Adult AIDS CRS Baltimore Maryland 21287
Beth Israel Deaconess Med. Ctr., ACTG CRS Boston Massachusetts 02215
Washington U CRS St Louis Missouri 63110
St. Louis ConnectCare, Infectious Diseases Clinic St Louis Missouri 63112
Beth Israel Med. Ctr. (Mt. Sinai) New York New York 10003
Univ. of Rochester ACTG CRS Rochester New York 14642
Unc Aids Crs Chapel Hill North Carolina 27514
Duke Univ. Med. Ctr. Adult CRS Durham North Carolina 27710
Univ. of Cincinnati CRS Cincinnati Ohio 45267
Hosp. of the Univ. of Pennsylvania CRS Philadelphia Pennsylvania 19104

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00000854, 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 Oct 28, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00000854 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →