Trial record 88 of 1236 for:    "Observational" [STUDY-TYPES] AND HIV [CONDITION]

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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01006005
Recruitment Status : Completed
First Posted : November 2, 2009
Last Update Posted : November 22, 2012
Information provided by (Responsible Party):
University of California, San Francisco

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.

Condition or disease
HIV Infections Adherence

Study Type : Observational
Actual Enrollment : 51 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Adherence-Suppression-Resistance Relationships for Atripla Compared to Historical Antiretroviral Regimens
Study Start Date : July 2007
Actual Primary Completion Date : June 2008
Actual Study Completion Date : June 2008

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS
Drug Information available for: Atripla

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
HIV infected, marginally housed

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.

Responsible Party: University of California, San Francisco Identifier: NCT01006005     History of Changes
Other Study ID Numbers: IN-US-177-0106
First Posted: November 2, 2009    Key Record Dates
Last Update Posted: November 22, 2012
Last Verified: November 2012

Keywords provided by University of California, San Francisco:
Treatment experienced

Additional relevant MeSH terms:
HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Anti-Retroviral Agents
Efavirenz, Emtricitabine, Tenofovir Disoproxil Fumarate Drug Combination
Antiviral Agents
Anti-Infective Agents
Reverse Transcriptase Inhibitors
Nucleic Acid Synthesis Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Anti-HIV Agents