Status:

COMPLETED

Psilocybin for Treatment of Obsessive Compulsive Disorder

Lead Sponsor:

University of Arizona

Conditions:

Obsessive-compulsive Disorder (OCD)

Eligibility:

All Genders

18-65 years

Phase:

PHASE1

Brief Summary

This study will evaluate whether psilocybin, a hallucinogenic drug, improves symptoms of obsessive compulsive disorder (OCD), whether it is safely tolerated as treatment of OCD, and will investigate t...

Detailed Description

The study seeks to improve our ability to treat and improve the lives of people who have obsessive-compulsive disorder (OCD) by exploring the benefits of psilocybin, a mind-altering drug that changes ...

Eligibility Criteria

Inclusion

  • Have moderate to severe OCD (DSM-5) after diagnostic interview using the Structured Clinical Interview for DSM-5 Research Version (SCID-R).
  • Failed at least one adequate attempted routine care treatment.
  • Considered safe for independent living

Exclusion

  • Concurrent psychosis, active substance use disorder, or a personal history of psychosis.
  • Medical illness based on physical examination and routine blood testing that may complicate cardiovascular safety or drug metabolism or excretion, such as uncontrolled hypertension, severe cardiac disease, or kidney or liver failure.
  • Unstable Chronic Obstructive Pulmonary Disease (COPD) or severe sleep apnea
  • Psychiatric comorbidity that may represent an acute risk to their own or others' safety.
  • Subjects may not be using antidepressant medication for OCD for at least two weeks before receiving study drug, and they cannot require any sedative, narcotic, or neuroleptic medications on a regular basis. Any of these medications they have taken should have been stopped long enough in the past to allow for their elimination and safe withdrawal prior to starting administration of the study drug. The specific time required will be dependent on the medication the patient was previously receiving.
  • Women who are pregnant, breastfeeding, or unwilling/unable to practice medically acceptable birth control during the study.
  • Allergy to lorazepam.

Key Trial Info

Start Date :

January 2 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 30 2023

Estimated Enrollment :

15 Patients enrolled

Trial Details

Trial ID

NCT03300947

Start Date

January 2 2019

End Date

December 30 2023

Last Update

August 30 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University of Arizona

Tucson, Arizona, United States, 85724