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CompletedNCT04192370

Cannabidiol for Craving During Buprenorphine Treatment

About this title

Cannabidiol Use to Reduce Cravings in Individuals With Opioid Use Disorder on Buprenorphine

Read the official source — NCT04192370
Medication studyAges 18–75United StatesAddiction
The study in practice

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Who was this study for?

Listed age limits: 18 years to 75 years.

Listed locations
BostonSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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Study clarity

Study information

Study start dateStarted: August 3, 2020
Recruitment status
Completed
Enrollment listed in the registry
8
Sponsor
Brigham and Women's Hospital
Sponsor type
Hospital / academic medical center
Study type
Drug
Intervention type
Drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
From 18 Years to 75 Years
Official registry ID
NCT04192370
Official title
Show the full official title

A Single-arm, Open-label Feasibility Pilot of Cannabidiol as an Adjunct to Sublingual Buprenorphine on Cue-induced Cravings Among Individuals With Opioid Use Disorder

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Recruitment & locations

Completed

Boston

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Brigham and Women's Hospital, a hospital or academic medical center.

Did this study involve medication?

Yes. The study involved medication, including Cannabidiol 600mg.

Who was this study for?

Listed age limits: 18 years to 75 years.

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