Psilocybin for Opioid Use Disorder in Patients on Methadone Maintenance With Ongoing Opioid Use

Brief Summary

This study will investigate whether psilocybin administered under supportive conditions can reduce illicit opioid use and improve quality of life in individuals with Opioid Use Disorder (OUD) in Methadone Maintenance Treatment (MMT) who are concurrently using other opioids illicitly.

Intervention / Treatment

  • Drug: Placebo
  • Drug: Psilocybin

Condition or Disease

  • Opioid Use Disorder

Phase

Study Design

Study type: Interventional
Status: Not yet recruiting
Study results: No Results Available
Age: 21 Years to 70 Years   (Adult, Older Adult)
Enrollment: 92 ()
Funded by: Other

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Clinical Trial Dates

Start date: Jun 01, 2022
Primary Completion: Feb 01, 2024
Completion Date: Dec 01, 2024
Study First Posted: Feb 16, 2022
Last Updated: Jun 02, 2022

Sponsors / Collaborators

Lead Sponsor: N/A
Responsible Party: N/A

This randomized double-blind placebo-controlled trial will investigate whether 2 doses of psilocybin administered under supportive conditions can reduce illicit opioid use (assessed by self-report and urine toxicology) and improve quality of life as measured by World Health Organization Quality of Life (WHOQOL-BREF) in individuals with OUD in MMT who are concurrently using other opioids illicitly. In addition, the investigators will investigate secondary outcomes including whether psilocybin under supportive conditions improves mood, reduces use of tobacco and other non-opioid drugs, improves chronic pain and sleep.

Ninety-two participants aged 21-70 who meet Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for OUD, are enrolled in a MMT program for at least 3 months, and have urine toxicology positive for methadone and another opioid will be recruited from the community and complete all study procedures. Participants will be randomized to an active group or control group (46 per group). Participants will undergo a total of 2 dosing sessions (whether psilocybin or placebo). The active group will receive 40mg psilocybin first. All participants will receive a second dosing session at three months. The active group will be further randomized, with half receiving 40mg psilocybin, and half receiving placebo at three months to test a secondary hypothesis that two doses of psilocybin are more effective in treating OUD than a single dose.

Eligibility Criteria

Sex: All

More Details

NCT Number: NCT05242029
Other IDs: IRB00251861
Study URL: https://ClinicalTrials.gov/show/NCT05242029
Last updated: Jun 17, 2022