RecruitingEarly Phase 1NCT04587791

Cannabidiol in Opioid Use Disorder and Chronic Pain

Cannabidiol Pharmacotherapy for Co-occurring Opioid Use Disorder and Chronic Pain


Sponsor

Yale University

Enrollment

34 participants

Start Date

Dec 8, 2021

Study Type

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

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called 1200 mg Cannabidiol, a drug called 400 mg Cannabidiol, and others for people with chronic pain and opioid-use disorder. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 70 Years.

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

DRUG400 mg Cannabidiol

Participants will receive 400 mg CBD

DRUG800 mg Cannabidiol

Participants will receive 800 mg CBD

DRUG1200 mg Cannabidiol

Participants will receive 1200 mg CBD

DRUGBeta carotene oral solution without CBD

Participants will receive beta carotene oral solution without CBD (placebo)


Locations(1)

Department of Veterans Affairs Hospital

West Haven, Connecticut, United States

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NCT04587791


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