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OpenTrials
Completed

NCT Number: NCT00096772

Collection of Blood Samples From HIV Infected People

The purpose of this study is to collect blood samples from HIV infected individuals for use in future genetic studies.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Dr. M. Estes Med. Practice CRS, Mill Valley, California, United States

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About this study

Genetic differences among people with HIV may account for differences in disease progression and response to antiretroviral therapy. The Terry Beirn Community Programs for Clinical Research on AIDS (CPCRA) was created to conduct studies in HIV infected communities and particularly in people of color, women, and injection drug users. This study will collect whole blood samples from HIV infected individuals. The samples will be used in future CPCRA studies comparing human genetic factors with clinical data from other CPCRA studies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Presently participating, previously participated in, or has given informed consent for participation in a qualifying CPCRA clinical trial
  • Signed informed consent

Sponsors and collaborators

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Nih

Registry information

Official study title

Collection and Use of Blood For Genetic and Other Related Analyses (The GENOMICS Protocol)

Important dates

Study start
2005
Primary completion
2007
Study completion
2007
First posted
Nov 16, 2004
Registry last updated
May 19, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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