Clinical Adverse Events In HIV-Infected Patients
Phase 4
N/A
N/A
N/A
N/A
Open (Enrolling by invite only)
Both
HIV, AIDS
Both
HIV, AIDS
Trial Information
Clinical Adverse Events In HIV-Infected Patients
All patients identified in the HIV registries will be included without any sampling
Inclusion Criteria:
- HIV infection.
Exclusion Criteria:
- None.
Type of Study:
Observational
Study Design:
Observational Model: Cohort, Time Perspective: Retrospective
Outcome Measure:
Incidence rate of Malignancies
Outcome Time Frame:
Median follow up of 3 years
Safety Issue:
Yes
Principal Investigator
Pfizer CT.gov Call Center
Investigator Role:
Study Director
Investigator Affiliation:
Pfizer
Authority:
United States: Investigational Review Board
Study ID:
A4001106
NCT ID:
NCT01339416
Start Date:
October 2008
Completion Date:
July 2013
Related Keywords:
- HIV
- AIDS
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