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Not listed Phase 3 Interventional

Comparing Side Effects of Two Forms of Videx in HIV-Infected Adults

ClinicalTrials.gov ID: NCT00008489

Public ClinicalTrials.gov record NCT00008489. 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, 2:16 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 Randomized Open-Label Trial Comparing the Tolerability of Videx EC Capsules to Videx Tablets in Adults With HIV Infection

Brief summary

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

The purpose of this study is to compare gastrointestinal (stomach and intestines) side effects of 2 forms of Videx in HIV-infected patients. Videx can be an effective anti-HIV treatment but many patients will not take the medication due to its side effects. Videx EC is a capsule form of the drug and may have fewer side effects. Also, patients would not have to take as many pills since patients taking Videx EC would have to take only 1 capsule per day instead of 2 tablets per day. This study will see if patients taking Videx EC have fewer side effects.

Study identification

NCT ID
NCT00008489
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
PharmaResearch
Industry
Enrollment
200 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
16 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
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 23, 2005

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Altamed Medical Health Services Los Angeles California 90022
Tower ID Med Associates Los Angeles California 90048
Pacific Horizons Med Group San Francisco California 94115
George Washington Univ Med Ctr Washington D.C. District of Columbia 20037
Community Research Initiative of South Florida Coral Gables Florida 33146
Atlanta VA Med Ctr Decatur Georgia 30033
Wayne State Univ - WSU/DMC / Univ Hlth Ctr Detroit Michigan 48201
Park Nicollet Med Ctr / Hlth Education Saint Louis Park Minnesota 55416
Treatment for Life Ctr Brooklyn New York 112123198
Jemsek Clinic Huntersville North Carolina 28078
Bornemann Internal Medicine Reading Pennsylvania 19601
Burnside Clinic Columbia South Carolina 29206
Julio Arroyo West Columbia South Carolina 29169
Univ of Texas Southwestern Med Ctr of Dallas Dallas Texas 75235
Hampton Roads Med Specialists Hampton Virginia 23666

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 NCT00008489, 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 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00008489 live on ClinicalTrials.gov.

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