drugset / Trial / NCT06067737

Outpatient Buprenorphine Induction With Psilocybin for Opioid Use Disorder

NCT06067737

Phase 2 Recruiting 90 enrolled Johns Hopkins University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2024-02-08
Primary completion
2028-07
Completion
2029-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator Psilocybin Other / unclassified 1 mg Oral
Comparator Psilocybin Other / unclassified 30 mg Oral