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Completed Phase 3 Interventional

Anti-HIV Drug Regimens With or Without Protease Inhibitors and Drug Level Monitoring in HIV Infected Adolescents

ClinicalTrials.gov ID: NCT00075907

Public ClinicalTrials.gov record NCT00075907. 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 2, 2026, 6:25 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 Comparative Trial of Protease-Containing and Protease-Sparing HAART Regimens in HIV-Infected Adolescents With an Evaluation of Therapeutic Drug Monitoring

Brief summary

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

The purpose of this study is to compare the effectiveness of anti-HIV drug regimens with or without a protease inhibitor (PI) in HIV infected adolescents. It will also determine if monitoring drug levels and adjusting the dose as necessary improves the effectiveness of these regimens.

Study identification

NCT ID
NCT00075907
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
240 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 Years to 23 Years
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
Jun 30, 2004
Primary completion
Not listed
Completion
Aug 31, 2006
Last update posted
Oct 6, 2013

2004 – 2006

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Usc La Nichd Crs Alhambra California 91803
Long Beach Memorial Med. Ctr., Miller Children's Hosp. Long Beach California 90806
Children's Hospital of Los Angeles NICHD CRS Los Angeles California 90027
Univ. of Colorado Denver NICHD CRS Aurora Colorado 80045
Chicago Children's CRS Chicago Illinois 60614
Tulane/LSU Maternal/Child CRS New Orleans Louisiana 70112
Children's Hosp. New Orleans Louisiana 70118
Johns Hopkins Hosp. & Health System - Dept. of Peds., Div. of Infectious Diseases Baltimore Maryland 21287
SUNY Stony Brook NICHD CRS Stony Brook New York 11794
Bronx-Lebanon Hosp. IMPAACT CRS The Bronx New York 10457
St. Jude/UTHSC CRS Memphis Tennessee 38105
Children's Med. Ctr. Dallas Dallas Texas 75235
Texas Children's Hosp. CRS Houston Texas 77030

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 NCT00075907, 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 6, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00075907 live on ClinicalTrials.gov.

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