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Adherence-Suppression-Resistance Relationships for Atripla Compared to Historical Antiretroviral Regimens

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Completed

Conditions

Adherence
HIV Infections

Study type

Observational

Funder types

Other

Identifiers

NCT01006005
IN-US-177-0106

Details and patient eligibility

About

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.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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