drugset / Trial / NCT04873453

CBD for the Treatment of Alcohol Use Disorder

NCT04873453 ↗

Phase 2 Completed 45 enrolled University of Colorado, Denver
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a double-blind, placebo-controlled, parallel group study designed to assess the efficacy of full spectrum cannabidiol (CBD) and broad spectrum CBD, compared to a placebo control (PC), to reduce drinking in participants with moderate alcohol use disorder according to the DSM-V. If eligible for the study, subjects will be randomized to receive one of the conditions for 8 weeks.

Timeline

Start
2021-08-30
Primary completion
2023-05-31
Completion
2023-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Cannabidiol Other / unclassified 150 mg —