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Completed Not applicable Interventional

Effect of Tenofovir Disoproxil Fumarate on Lipid Levels in HIV Infected Adults on Stable Anti-HIV Drug Therapy

ClinicalTrials.gov ID: NCT00109603

Public ClinicalTrials.gov record NCT00109603. 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, 1:15 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 Pilot Study to Determine the Impact on Dyslipidemia of the Addition of Tenofovir to Stable Background Antiretroviral Therapy in HIV-Infected Subjects

Brief summary

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

The purpose of this study is to determine the effect of the anti-HIV drug tenofovir disoproxil fumarate (TDF) on lipid levels in HIV infected adults on stable anti-HIV drug therapy. Study hypothesis: The addition of TDF to stable background antiretroviral therapy in HIV infected individuals with dyslipidemia will result in a reduction of non-HDL after 12 weeks of treatment.

Study identification

NCT ID
NCT00109603
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
17 participants

Conditions and interventions

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
Apr 30, 2005
Primary completion
Jun 30, 2007
Completion
Oct 31, 2007
Last update posted
Oct 29, 2012

2005 – 2007

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
University of Southern California Los Angeles California 90033-1079
University of California, San Diego Antiviral Research Center San Diego California 92103
University of Colorado Health Sciences Center, Denver Denver Colorado 80262-3706
University of Miami Miami Florida 33136-1013
Indiana University Hospital Indianapolis Indiana 46202-5250
Methodist Hospital of Indiana Indianapolis Indiana 46202-5250
Wishard Hospital Indianapolis Indiana 46202
University of Maryland, Institute of Human Virology Baltimore Maryland 21201
Johns Hopkins University Baltimore Maryland 21287-8106
Washington University (St. Louis) St Louis Missouri 63108-2138
Beth Israel Medical Center New York New York 10003
NYU/Bellevue New York New York 10016-6481
Duke University Medical Center Durham North Carolina
University of Cincinnati Cincinnati Ohio 45267-0405
Case Western Reserve University Cleveland Ohio 44106-5083
MetroHealth Medical Center Cleveland Ohio 44109-1998
University of Pennsylvania, Philadelphia Philadelphia Pennsylvania 19104
University of Pittsburgh Pittsburgh Pennsylvania 15213-2582
University of Texas, Galveston Galveston Texas 77555-0435

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00109603, 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 29, 2012 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00109603 live on ClinicalTrials.gov.

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