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Outpatient Buprenorphine Induction With Psilocybin for Opioid Use Disorder: a Randomized Double-blind Trial

This study will examine the effect of a single high dose of psilocybin therapy (30 mg) versus a very low dose (1 mg) as an adjunctive therapy to individuals undergoing standard-of-care outpatient buprenorphine treatment for Opioid use disorder (OUD). The participants will have previously undergone buprenorphine induction before. Effects of adjunctive psilocybin will be determined for longitudinal outcomes of opioid abstinence, compliance with outpatient buprenorphine maintenance, quality of life, and mood.

Status
recruiting
Phase
Phase 2
Institution
Johns Hopkins University
Principal investigator
Sandeep Nayak, MD
Start date
2024-02-08
End date
2029-05-01
Registry ID
NCT06067737

View trial record

Tracked by the DMT Code Clinical Trials Observatory, an open record of DMT-related clinical research.