Cannabidiol in Opioid Use Disorder and Chronic Pain
Cannabidiol Pharmacotherapy for Co-occurring Opioid Use Disorder and Chronic Pain
Yale University
34 participants
Dec 8, 2021
INTERVENTIONAL
Conditions
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.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
Participants will receive 400 mg CBD
Participants will receive 800 mg CBD
Participants will receive 1200 mg CBD
Participants will receive beta carotene oral solution without CBD (placebo)
Locations(1)
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NCT04587791