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Completed Phase 2 Interventional

The Effects of Prednisone on HIV Levels and the Immune System

ClinicalTrials.gov ID: NCT00000921

Public ClinicalTrials.gov record NCT00000921. 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 Oct 4, 2026, 12:18 AM 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 Phase II, Randomized, Placebo-Controlled Study of the Immunologic and Virologic Effects of Prednisone on HIV-1 Infection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to see if it is safe and effective to give prednisone to HIV-infected patients. Prednisone is a corticosteroid, a hormone produced by the body that inhibits immune cell responses. Prednisone may be able to lower the level of HIV in the body (viral load) by reducing the number of cells that HIV can infect. At the same time, prednisone may be able to increase CD4 cell counts (cells of the immune system that fight infection).

Study identification

NCT ID
NCT00000921
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
118 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Aug 1996 (Type not available)
Primary completion
Jun 2002 (Actual)
Completion
Not listed
Last update posted
Feb 23, 2011

Started 1996

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Univ of Alabama at Birmingham Birmingham Alabama 35294 —
Univ of Southern California / LA County USC Med Ctr Los Angeles California 900331079 —
Queens Med Ctr Honolulu Hawaii 96816 —
Univ of Hawaii / Leahi Hosp Honolulu Hawaii 96816 —
Univ of Hawaii Honolulu Hawaii 96816 —
Northwestern Univ Med School Chicago Illinois 60611 —
Cook County Hosp Chicago Illinois 60612 —
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612 —
Indiana Univ Hosp Indianapolis Indiana 462025250 —
Harvard (Massachusetts Gen Hosp) Boston Massachusetts 02114 —
Univ of Minnesota Minneapolis Minnesota 55455 —
Bellevue Hosp / New York Univ Med Ctr New York New York 10016 —
Mount Sinai Med Ctr New York New York 10029 —
Case Western Reserve Univ Cleveland Ohio 44106 —
MetroHealth Med Ctr Cleveland Ohio 441091998 —
Ohio State Univ Hosp Clinic Columbus Ohio 432101228 —
Milton S Hershey Med Ctr Hershey Pennsylvania 170330850 —
Univ of Washington Seattle Washington 98104 —

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 NCT00000921, 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 Feb 23, 2011 · Synced Oct 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00000921 live on ClinicalTrials.gov.

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