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Completed Not applicable Interventional

Safety, Effectiveness, and Tolerability of Ezetimibe Combined With Statins for the Treatment of High Cholesterol in HIV Infected Adults

ClinicalTrials.gov ID: NCT00099684

Public ClinicalTrials.gov record NCT00099684. 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 18, 2026, 4:12 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 of the Safety, Efficacy, and Tolerability of Ezetimibe (Zetia) in Combination With Statin Therapy for the Treatment of Elevated LDL Cholesterol in HIV-Infected Subjects

Brief summary

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

Anti-HIV drugs, especially protease inhibitors (PIs), have been linked to lipid metabolism problems, including elevations in low density lipoprotein cholesterol (LDL-c), triglycerides, and total cholesterol. Ezetimibe is a lipid-controlling drug; statins are part of another class of lipid-lowering drugs popularly prescribed to people with high cholesterol. The purpose of this study is to determine the safety, effectiveness, and tolerability of ezetimibe in combination with statin therapy in adults who are taking anti-HIV drugs and have high cholesterol. Study hypothesis: In HIV infected adults, ezetimibe in combination with statin therapy will result in significantly lower LDL-c compared to statin therapy alone.

Study identification

NCT ID
NCT00099684
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
44 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
Nov 2005 (Type not available)
Primary completion
Not listed
Completion
May 2007 (Actual)
Last update posted
Oct 29, 2012

2005 – 2007

United States locations

U.S. sites
41
U.S. states
17
U.S. cities
27
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35924-2050 —
UCLA School of Medicine Los Angeles California 77555-0435 —
University of Southern California Los Angeles California 90033-1079 —
University of California, San Diego Antiviral Research Center San Diego California 92103 —
San Francisco General Hospital San Francisco California 94110 —
San Mateo County AIDS Program Stanford California 94305-5107 —
Santa Clara Valley Medical Center Stanford California 94305-5107 —
Stanford University Stanford California 94305-5107 —
Willow Clinic Stanford California 94305-5107 —
Georgetown University Medical Center Washington D.C. District of Columbia 20007 —
University of Miami Miami Florida 33136-1013 —
University of Hawaii Honolulu Hawaii 96816-2396 —
Rush-Presbyterian/St. Lukes (Chicago) Chicago Illinois 60611-3015 —
Cook County Hospital Core Center Chicago Illinois 60612 —
Feinberg School of Medicine, HIV/ACTU Chicago, 60611-3015 Illinois 60611-3015 —
Indiana University Hospital Indianapolis Indiana 46202-5250 —
Wishard Hospital Indianapolis Indiana 46202 —
University of Minnesota Minneapolis Minnesota 55455-0392 —
Nebraska Health System Omaha Nebraska 68198-5130 —
SUNY - Buffalo (Rochester) Buffalo New York 14215 —
Beth Israel Medical Center New York New York 10003 —
Chelsea Clinic New York New York 10011 —
NYU/Bellevue New York New York 10016-6481 —
The Cornell Clinical Trials Unit New York New York 10021 —
Columbia University New York New York 10032-3784 —
Community Health Network, Inc. Rochester New York 14642-0001 —
University of Rochester Medical Center Rochester New York 14642-0001 —
Duke University Medical Center Durham North Carolina — —
University of Cincinnati Cincinnati Ohio 45267-0405 —
MetroHealth Medical Center Cleveland Ohio 44109-1998 —
Ohio State University Columbus Ohio 43210 —
Presbyterian Medical Center - Univ. of PA Philadelphia Pennsylvania 19104 —
University of Pennsylvania, Philadelphia Philadelphia Pennsylvania 19104 —
University of Pittsburgh Pittsburgh Pennsylvania 15213-2582 —
Rhode Island Hospital Providence Rhode Island 02906 —
Stanley Street Treatment and Resource Providence Rhode Island 02906 —
The Miriam Hospital Providence Rhode Island 02906 —
Comprehensive Care Clinic Nashville Tennessee 37203 —
Dallas VA Medical Center Dallas Texas 75235-9173 —
University of Texas, Galveston Galveston Texas 77555-0435 —
University of Washington (Seattle) 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.

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 NCT00099684, 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 Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00099684 live on ClinicalTrials.gov.

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