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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 Sep 2, 2026, 5:36 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 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
Oct 31, 2005
Primary completion
Not listed
Completion
Apr 30, 2007
Last update posted
Oct 28, 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 28, 2012 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00099684 live on ClinicalTrials.gov.

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