About this trial
The goal of this pilot study is to test novel, adjunctive pharmacotherapy for patients with opioid use disorder (POUD) who may be at risk for overdose and other poor opioid use disorder (OUD) outcomes even after initiating buprenorphine. The investigator team proposes to test the effectiveness of combined dronabinol (synthetic delta-9-tetrahydrocannabinol \[THC\]) and Epidiolex (cannabidiol \[CBD\]) - two FDA-approved cannabinoids - to improve retention in buprenorphine treatment and reduce opioid use among POUD who are early in treatment. POUD who are early in treatment are at a critical juncture-a moment of opportunity and motivation, but also of high risk of return to opioid use and loss to follow up.
Eligibility criteria
Qualifiers
Fluency in English and Spanish
The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnosis of OUD
Newly initiated on buprenorphine within 21 days
Positive urine toxicology for opioids other than buprenorphine in the past week OR opioid withdrawal symptoms in the past week based on the Clinical Opioid Withdrawal Scale (COWS) >=5
Disqualifiers
Urine toxicology positive for cannabinoids
Inability to provide informed consent
Liver tests (AST or ALT) >3 times the upper limit of normal, or a history of liver disease
Pregnancy or breast/chest feeding
Trial design
Treatments tested in this trial
- Dronabinol Capsules
- Epidiolex 100 mg/mL Oral Solution
- Placebo Dronabinol
- Placebo Epidiolex
Treatment groups
Sponsors and collaborators
Montefiore Medical Center
Lead sponsor
National Institute on Drug Abuse (NIDA)
Collaborator