Overview

Epidiolex in Obsessive Compulsive Disorder

Status:
Not yet recruiting
Trial end date:
2023-09-01
Target enrollment:
0
Participant gender:
All
Summary
The goal of the proposed study is to evaluate the safe and efficacy of Epidiolex (cannabidiol) in adults with obsessive compulsive disorder (OCD). Subjects will be treated in an open-label fashion with Epidiolex for two weeks.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Chicago
Treatments:
Cannabidiol
Epidiolex
Criteria
Inclusion Criteria:

- Men and women age 18-65

- Primary diagnosis of OCD

- YBOCS score of at least 18 at baseline

- Ability to understand and sign the consent form.

Exclusion Criteria:

- Unstable medical illness based on history or clinically significant abnormalities on
baseline physical examination or labs

- Current pregnancy or lactation, or inadequate contraception in women of childbearing
potential

- Subjects considered an immediate suicide risk based on the Columbia Suicide Severity
Rating Scale (C-SSRS)

- Past 12-month DSM-5 psychiatric disorder other than OCD

- Illegal substance use based on urine toxicology screening

- Initiation of psychological interventions within 3 months of screening

- Use of any other psychotropic medication

- Previous treatment with epidiolex

- Cognitive impairment that interferes with the capacity to understand and
self-administer medication or provide written informed consent