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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01006005

Enrollment

Registered

2009-11-02

Start date

2007-07-31

Completion date

2008-06-30

Last updated

2023-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adherence, HIV Infections

Keywords

HIV, Treatment experienced

Brief 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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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.

Outcome results