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Completed Not applicable Interventional

Long-Term Assessment for Metabolic, Cardiovascular and Neurologic Problems in HIV-Infected Patients With Increased CD4 Cells Counts Following Anti-HIV Therapy

ClinicalTrials.gov ID: NCT00000883

Public ClinicalTrials.gov record NCT00000883. 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 23, 2026, 7:44 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

Long-Term Assessment for Metabolic, Cardiovascular and Neurologic Complications In Subjects With Past CD4 Cells/mm3 Below 50 Who Increased CD4 Cells/mm3 to Above 100 on HAART

Brief summary

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

The purpose of this study is to see if there are any changes in sugar and fat levels in the blood when patients take anti-HIV therapy for many years. Another goal is to test memory and mental concentrations to determine if anti-HIV drugs protect the brain from damage caused by HIV. (The purpose of this study has been changed from the original version.) HIV-infected patients with low CD4 cell counts are at risk for getting opportunistic (AIDS-related) infections. CD4 cells are cells of the immune system that help fight infection. Anti-HIV therapy may increase CD4 counts, which may lead to a decrease in AIDS-related infections. Problems that anti-HIV therapy is associated with include metabolic problems, neurologic problems, abnormal opportunistic infections, and cancer. Patients in ACTG 362 have been exposed to anti-HIV therapy longer than any other large group in the ACTG. These patients appear to benefit from their therapy, but also suffer problems from it. Observation of these patients should provide more information about long-term anti-HIV treatment and may detect unexpected problems. (This study as been changed. More information about the reasons for conducting this study has been added.)

Study identification

NCT ID
NCT00000883
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
636 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 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 1997 (Type not available)
Primary completion
Not listed
Completion
Apr 2007 (Actual)
Last update posted
Oct 25, 2012

1997 – 2007

United States locations

U.S. sites
51
U.S. states
22
U.S. cities
34
Facility City State ZIP Site status
Univ of Alabama at Birmingham Birmingham Alabama 35294 —
Univ of Southern California / LA County USC Med Ctr Los Angeles California 900331079 —
Willow Clinic Menlo Park California 94025 —
Univ of California / San Diego Treatment Ctr San Diego California 921036325 —
San Francisco Gen Hosp San Francisco California 941102859 —
Stanford at Kaiser / Kaiser Permanente Med Ctr San Francisco California 94115 —
Santa Clara Valley Med Ctr / AIDS Community Rsch Consortium San Jose California 951282699 —
San Mateo AIDS Program / Stanford Univ Stanford California 943055107 —
Stanford Univ Med Ctr Stanford California 943055107 —
Harbor UCLA Med Ctr Torrance California 90502 —
Univ of Colorado Health Sciences Ctr Denver Colorado 80262 —
Howard Univ Washington D.C. District of Columbia 20059 —
Emory Univ Atlanta Georgia 30308 —
Emory Hemo Comp Evaluation Clinic / East TN Comp Hemo Ctr Atlanta Georgia 303652225 —
Queens Med Ctr Honolulu Hawaii 96816 —
Univ of Hawaii Honolulu Hawaii 96816 —
Northwestern Univ Med School Chicago Illinois 60611 —
Cook County Hosp Chicago Illinois 60612 —
Rush Presbyterian - Saint Luke's Med Ctr Chicago Illinois 60612 —
Louis A Weiss Memorial Hosp Chicago Illinois 60640 —
Indiana Univ Hosp Indianapolis Indiana 462025250 —
Division of Inf Diseases/ Indiana Univ Hosp Indianapolis Indiana 46202 —
Methodist Hosp of Indiana / Life Care Clinic Indianapolis Indiana 46202 —
Charity Hosp / Tulane Univ Med School New Orleans Louisiana 70112 —
Johns Hopkins Hosp Baltimore Maryland 21287 —
Harvard (Massachusetts Gen Hosp) Boston Massachusetts 02114 —
Boston Med Ctr Boston Massachusetts 02118 —
Beth Israel Deaconess - West Campus Boston Massachusetts 02215 —
Beth Israel Deaconess Med Ctr Boston Massachusetts 02215 —
Univ of Minnesota Minneapolis Minnesota 55455 —
St Louis Regional Hosp / St Louis Regional Med Ctr St Louis Missouri 63112 —
Univ of Nebraska Med Ctr Omaha Nebraska 681985130 —
SUNY / Erie County Med Ctr at Buffalo Buffalo New York 14215 —
Beth Israel Med Ctr New York New York 10003 —
Bellevue Hosp / New York Univ Med Ctr New York New York 10016 —
Cornell Univ Med Ctr New York New York 10021 —
Mem Sloan - Kettering Cancer Ctr New York New York 10021 —
Mount Sinai Med Ctr New York New York 10029 —
Community Health Network Inc Rochester New York 14642 —
Univ of Rochester Medical Center Rochester New York 14642 —
Univ of North Carolina Chapel Hill North Carolina 275997215 —
Duke Univ Med Ctr Durham North Carolina 27710 —
Univ of Cincinnati Cincinnati Ohio 452670405 —
Case Western Reserve Univ Cleveland Ohio 44106 —
Ohio State Univ Hosp Clinic Columbus Ohio 432101228 —
Univ of Pennsylvania at Philadelphia Philadelphia Pennsylvania 19104 —
Univ of Pittsburgh Med Ctr Pittsburgh Pennsylvania 15213 —
Julio Arroyo West Columbia South Carolina 29169 —
Univ of Tennessee / E Tennessee Comprehensive Hemophilia Ctr Knoxville Tennessee 37920 —
Univ of Texas Galveston Galveston Texas 775550435 —
Univ of Washington Seattle Washington 981224304 —

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 NCT00000883, 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 25, 2012 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00000883 live on ClinicalTrials.gov.

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