Cannabinoid Medication for Adults With OCD

Completed · Phase 1/Phase 2

Conditions studied: Obsessive-Compulsive Disorder

In brief

The purpose of this pilot research study is to test the effects of a medication called nabilone (Cesamet) in adults with obsessive-compulsive disorder (OCD). Participants will receive either nabilone on its own, or nabilone in combination with a form of cognitive-behavioral therapy (CBT) called exposure and response prevention (EX/RP). Nabilone is a synthetic cannabinoid and acts on the brain's "endocannabinoid system," which has been hypothesized to play a role in OCD. Nabilone is approved by the FDA for the treatment of chemotherapy-induced nausea and vomiting. It is not FDA-approved for treating OCD.

Key facts

Study ID
NCT02911324
Run by
New York State Psychiatric Institute
People needed
16
Starts
2016-09-01
Expected to finish
2019-01-01
Last updated by the study team
2020-08-06

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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