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

PHASE2CompletedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

August 3, 2020

Primary Completion Date

December 30, 2021

Study Completion Date

December 30, 2021

Conditions
Opioid-use Disorder
Interventions
DRUG

Cannabidiol 600mg

All subjects will receive 600mg of oral cannabidiol for 3 days in an open-label fashion. Cannabidiol will be provided using Epidiolex™ oral solution 100mg/mL, and the drug will be procured by the Brigham and Women's Hospital (BWH) Investigational Drug Services (IDS) pharmacy. The first dose will be administered at the BWH Center for Clinical Investigation, while doses 2 and 3 will be self-administrated at home. The CBD will be repacked in pre-drawn syringes for the subjects to self-administer at home.

Trial Locations (1)

02115

Brigham and Women's Hospital, Boston

All Listed Sponsors
lead

Brigham and Women's Hospital

OTHER

NCT04192370 - Cannabidiol Use to Reduce Cravings in Individuals With Opioid Use Disorder on Buprenorphine | Biotech Hunter | Biotech Hunter