drugset / Trial / NCT04587791
Cannabidiol in Opioid Use Disorder and Chronic Pain
Phase 0
Recruiting
34 enrolled
Yale University
National Institute on Drug Abuse (NIDA) · collabVA Connecticut Healthcare System · collab
RandomizedCrossoverDouble-blindTreatment
Summary
This is a randomized, placebo-controlled, crossover human laboratory study investigating the dose-dependent safety and acute effects of Cannabidiol (CBD) on measures of pain and opioid craving in outpatients with opioid use disorder (OUD) receiving medication-assisted treatment with methadone or buprenorphine. With a duration of approximately 4 weeks, participants will come to the testing site for a total of five times: one initial screening session, and four experimental sessions where study medication, CBD, will be administered, separated by at least 72 hours to limit carryover effects.
Timeline
- Start
- 2021-12-08
- Primary completion
- 2026-08-31
- Completion
- 2026-08-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Cannabidiol | Other / unclassified | 400 mg | Oral |
| Comparator | Cannabidiol | Other / unclassified | 800 mg | Oral |
| Comparator | Cannabidiol | Other / unclassified | 1200 mg | Oral |