Comparison of HIV Clinic-based Treatment With Buprenorphine Versus Referred Care in Heroin-dependent Participants
Opiate Dependence, HIV Seropositivity, HIV Infections
About this trial
This is an interventional treatment trial for Opiate Dependence focused on measuring Drug Dependence, Opiate Dependence, Human Immunodeficiency Viruses, Buprenorphine
Eligibility Criteria
Inclusion Criteria: HIV-infected and receiving continuity care in the Johns Hopkins HIV Clinic 18 years of age or older Meets DSM-IV criteria for opioid dependence Seeks agonist-based treatment for opioid dependence Willing and able to provide written informed consent Willing to be contacted by mail and telephone for study follow-up visit reminders Willing to authorize release of information for substance abuse treatment to the study for a period of 12 months If female, negative urine pregnancy test and willingness to practice birth control while on study if sexually active (barrier method or progesterone-containing contraception product) Verbal approval from participant's primary HIV clinician Exclusion Criteria: Currently receiving methadone, naloxone, buprenorphine, or levomethadyl acetate (LAAM) as part of a licensed opioid treatment program History of allergic reaction to buprenorphine or naloxone Active medical need for opioid-based pain control Active benzodiazepine abuse or dependence Active alcohol dependence Alanine aminotransferase level that is more than 5 times the upper limit of normal Other condition that, in the opinion of the principal investigator, makes participation in the study unsafe or follow-up highly unlikely
Sites / Locations
- Johns Hopkins HIV Clinic
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
1
2
Subjects receive integrated opioid-dependence treatment with buprenorphine/naloxone at the HIV clinic
Subjects receive case management and referral to an off-site opioid treatment program for their opioid dependence