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NOT YET RECRUITING
NCT07406828
PHASE1

Psilocybin After Trauma Surgery for Pain

Sponsor: Trent Emerick

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to evaluate whether a single dose of psilocybin is feasible and safe for adults with opioid use disorder (OUD) who are recovering from trauma surgery. The main questions it aims to answer are: 1. Is a single psilocybin dose feasible to administer during postoperative hospitalization? 2. Is psilocybin safe in this patient population? 3. How does psilocybin affect postoperative pain, opioid use, anxiety, and depression after hospital discharge? Participants will: Receive one oral dose of psilocybin during their postoperative inpatient stay Complete assessments of pain, mood, and opioid use during recovery

Official title: Single Dose Psilocybin for a Post-surgical Trauma Inpatient Population for Pain, Mood, and Opioid Use Disorder

Key Details

Gender

All

Age Range

25 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2026-07

Completion Date

2027-08

Last Updated

2026-02-12

Healthy Volunteers

No

Interventions

DRUG

Psilocybin (Usona Institute)

Single oral dose of psilocybin (10 mg) administered once during inpatient hospitalization to postoperative trauma surgery patients with opioid use disorder, followed by an 8-hour monitored observation period.

DRUG

Postoperative analgesia

Standard postoperative pain management, including multimodal analgesia and medications for opioid use disorder, provided per institutional clinical practice.

Locations (1)

UPMC Presbyterian

Pittsburgh, Pennsylvania, United States