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Not listed Phase 3 Interventional

Differences Between Women and Men Taking a Combination of Indinavir, Ritonavir, Enteric-Coated Didanosine, and Stavudine Who Previously Took Anti-HIV Drugs

ClinicalTrials.gov ID: NCT00006397

Public ClinicalTrials.gov record NCT00006397. 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 Sep 3, 2026, 5:00 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 Study of the Combination of Indinavir, Ritonavir, Enteric-Coated ddI and d4T In Nucleoside and Non-Nucleoside Reverse Transcriptase Inhibitor Experienced Patients: An Open-Label Study Investigating Differences Between Women and Men

Brief summary

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

The purpose of this study is to see how safe and effective it is to give multi-drug treatment with indinavir (IDV) plus ritonavir (RTV) plus enteric-coated didanosine (ddI) plus stavudine (d4T) and if there are differences in responses between men and women.

Study identification

NCT ID
NCT00006397
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
PPD Development, LP
Industry
Enrollment
200 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
Jul 31, 2000
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 23, 2005

Started 2000

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
East Bay AIDS Ctr Berkeley California 94705
Univ of Southern California Los Angeles California 90033
UCLA CARE Ctr Los Angeles California 90095
North Broward Hosp District / HIV Clinical Research Fort Lauderdale Florida 33311
Saint Josephs Comprehensive Research Institute Tampa Florida 33607
Louisiana State Univ Med Ctr / HIV Outpatient Clinic New Orleans Louisiana 70112
JSI Research and Training Institute Boston Massachusetts 02210
Univ of Med & Dentistry of New Jersey Newark New Jersey 07103
Beth Israel Med Ctr New York New York 10003
Harlem Hosp Ctr New York New York 10037
Univ of Rochester Med Ctr Rochester New York 14642
Vanderbilt Univ School of Medicine Nashville Tennessee 37212
Univ of Texas Southwestern Med Ctr Dallas Texas 75390

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 NCT00006397, 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 Jun 23, 2005 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00006397 live on ClinicalTrials.gov.

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