Optimizing Outcomes Using Suboxone for Opiate Dependence (OpBup)
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About
Building on a platform of pharmacological treatment with Suboxone (buprenorphine and naloxone), participants are randomly assigned to one of four psychosocial treatment conditions.
Full description
The approval of buprenorphine (combined with naloxone as Suboxone®) by the FDA enables physicians in the United States to provide pharmacotherapy treatment to opioid-dependent patients in private medical settings. Buprenorphine's wide acceptance and implementation by physicians has been slower than expected, however, and this may be due in part to the nature and necessity of providing comprehensive treatment for opioid-dependent patients. Lessons learned from methadone maintenance make it clear that simply providing opioid substitution does not address the behavioral components of dependence. While there is no lack of behavioral treatment facilities for substance abuse in the United States, what is lacking is an integrative approach to the treatment of opioid dependence using pharmacotherapy in conjunction with proven behavioral treatment strategies. Following a two-week stabilization and baseline period, this project will randomize 240 participants into 4 behavioral treatment groups featuring cognitive behavioral therapy and contingency management therapy. A universal, manual-guided psychosocial standard of care for buprenorphine pharmacological treatment allows for ethical inclusion of a "no-CBT or CM therapy" condition and closely resembles the current standard of psychosocial care delivered with opioid treatment using Suboxone®. Behavioral therapies will be delivered for 16 weeks (to study week 18) in conjunction with continued care with Suboxone®. An additional 16 weeks of treatment using Suboxone® (to study week 34) will ensue during which no CBT or CM therapies are provided. All participants enter a buprenorphine taper and return at study week 52 for long-term follow-up evaluations. Outcomes for the trial include illicit drug use (urine drug samples collected three times per week during the first 18 weeks), drug craving, retention (days in the protocol), psychiatric status (depression, mood), HIV risk behaviors, and treatment feasibility ratings. Results will be used to recommend strategies to optimize buprenorphine treatment outcomes and promote integration of pharmacotherapy and psychosocial/behavioral treatment strategies for physicians and for behavioral treatment facilities treating opioid-dependent patients.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Participants must:
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Be 15 years of age or older.
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Meet DSM-IV-TR criteria for opioid dependence.
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Be interested in receiving buprenorphine treatment for their opioid dependence.
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Be in good general health or, in case of a medical/psychiatric condition needing ongoing treatment, be under the care of a physician who provides documented willingness to continue participant's medical management and coordinate care with the study physicians. *
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Be agreeable to and capable of signing an informed consent.
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Have means of reliable transportation over the study period.
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If female and of child bearing potential, agree to use of one of the following methods of birth control or be surgically sterile:
- oral contraceptives
- patch
- barrier (diaphragm or condom)
- intrauterine contraceptive system
- levonorgestrel implant
- medroxyprogesterone acetate contraceptive injection
- complete abstinence from sexual intercourse
- hormonal vaginal contraceptive ring
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Be agreeable to and capable of complying with study procedures.
Exclusion criteria
Participants must not:
- Have a known sensitivity to buprenorphine or naloxone.
- Be dependent on alcohol, benzodiazepines or other drugs of abuse that require immediate medical attention.
- Have a medical condition that would, in the opinion of the study physician, make participation medically hazardous (e.g., acute hepatitis, unstable cardiovascular, liver or renal disease).
- Have a current pattern of benzodiazepine use, as assessed by the study physician, which would preclude safe participation in the study.
- Be actively involved in another clinical trial.
- Be acutely psychotic, severely depressed, and in need of inpatient treatment, or is an immediate suicide risk.
- Be a nursing or pregnant female. Females who become pregnant during the course of the study will be withdrawn from the study and referred to an appropriate treatment venue; i.e. narcotic treatment program or specialty addiction clinic.
- Be a female of childbearing potential who does not agree to use a medically acceptable method of birth control, e.g. oral contraceptives, barrier (diaphragm or condom) with or without spermicide, levonorgestrel implant, intra-uterine progesterone contraceptives system, medroxyprogesterone acetate contraceptive injection, or complete abstinence.
- Have any pending legal action that could prohibit continued participation for the one-year period of study participation (such as that which could possibly result in incarceration).
- Be expecting to leave the clinic's geographic area prior to study completion (within one year).
- Have been previously randomized to a treatment condition in this study. -
Trial design
Primary purpose
Allocation
Interventional model
Masking
202 participants in 4 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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