drugset / Trial / NCT04656301

Safety and Efficacy of Psilocybin for Body Dysmorphic Disorder

NCT04656301 ↗

NaSingle-groupOpen-labelTreatment

Summary

In this pilot study 12 adult outpatients with body dysmorphic disorder that has not responded to at least one adequate trial of a serotonin reuptake inhibitor will be treated openly with a single oral dose of psilocybin. Followup visits to monitor safety and clinical outcome will be conducted over a 3 month period.

Timeline

Start
2021-02-26
Primary completion
2022-11-02
Completion
2022-11-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Psilocybin Other / unclassified 25 mg Oral