Integrating Buprenorphine Into the SFGH AIDS Program
Completed · Phase 4
Conditions studied: HIV, Buprenorphine, Opioid Dependence
In brief
The purpose of this study is to assess the feasibility, cost, and effectiveness of a model of care designed to integrate buprenorphine treatment for opioid dependence into the HIV primary care clinics at the UCSF Positive Health Program.
Key facts
- Study ID
- NCT00263458
- Run by
- University of California, San Francisco
- People needed
- 37
- Starts
- 2005-12-01
- Expected to finish
- 2009-06-01
- Last updated by the study team
- 2011-09-12
Who can join
Age: 19 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age > 18 years
- Fluent in English
- Receive HIV primary care at the UCSF Positive Health Program
- Meet DSM-IVR criteria for opioid dependence
- Meet clinical criteria for buprenorphine treatment (see Exclusion Criteria)
- Plan to stay in the San Francisco Bay Area for the next 12 months
You may not qualify if…
- Severe hepatic dysfunction, i.e., AST and/or ALT > 5X upper limit of normal
- DSM-IV criteria for benzodiazepine abuse or dependence within the past 6 months
- DSM-IV criteria for alcohol dependence within the past 6 months
- Actively suicidal
- Psychiatric impairment that impedes ability to consent (dementia, delusional, actively psychotic)
- Methadone or opiate analgesic doses exceed level allowing for safe transition to buprenorphine
- Pregnant women and women actively trying to become pregnant
- Potential subjects also will be excluded for:
- Any medical condition(s), which, in the opinion of the investigator, would interfere with the patient's ability to participate in or adhere to the requirements of this study
- Unable or who decline to provide informed consent for the evaluation
Where it is running
- UCSF Positive Health Program — San Francisco, California, United States
Full record on ClinicalTrials.gov
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