Evaluation of Interferon-gamma Responses to HCMV Infection in HIV Positive Individuals

This study has been completed.
Sponsor:
Collaborator:
Cellestis
Information provided by (Responsible Party):
Jennifer Hoy, The Alfred
ClinicalTrials.gov Identifier:
NCT00168259
First received: September 13, 2005
Last updated: January 19, 2012
Last verified: January 2012

September 13, 2005
January 19, 2012
December 2004
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Complete list of historical versions of study NCT00168259 on ClinicalTrials.gov Archive Site
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Evaluation of Interferon-gamma Responses to HCMV Infection in HIV Positive Individuals
Evaluation of Interferon-gamma Responses to HCMV Infection in HIV Positive Individuals

The study is designed to evaluate interferon responses to CMV in HIV positive individuals and a component will look at interferon responses to CMV in HIV positive individuals over time after commencement of antiretroviral therapy. We will also look at the correlation between CD4 T cell numbers and HLA type with the interferon response.

Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
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Retention:   Samples With DNA
Description:

Plasma, and DNA

Non-Probability Sample

HIV infected patients with past CMV infection initiating antiretroviral therapy

  • HIV Infection
  • CMV Infection
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
December 2009
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Inclusion Criteria:

  1. HIV positive with history of documented HCV infection
  2. Over 18 years old
  3. HIV positive
  4. Antiretroviral naive, starting on antiretroviral therapy
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Australia
 
NCT00168259
185/04
No
Jennifer Hoy, The Alfred
The Alfred
Cellestis
Principal Investigator: Sharon Lewin, Professor The Alfred
The Alfred
January 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP