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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01006005
Other study ID # IN-US-177-0106
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2007
Est. completion date June 2008

Study information

Verified date November 2023
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study is recruiting 50 patients initiating or switching to Atripla and comparing them to 250 individuals previously followed in a prospective study of HIV+ low income individuals recruited from homeless shelters, single room occupancy hotels and free meal food lines as part of the UCSF Reach Study. Adherence will be measured through monthly unannounced pill counts and electronic medication monitors.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18+ years old; - HIV+; - Initiating Atripla within 6-months of recruitment; - Lives in the Tenderloin, South of Market, or Mission District San Francisco; - Capable of providing informed consent; and - Willing to complete all study procedures. Exclusion Criteria: - Intoxication, cognitive dysfunction or psychosis will preclude potential subjects from informed consent.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco
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