Efficacy of Nitrous Oxide in OCD: Pilot Study
Part of paid clinical trials in Stanford, California.
- Sponsor
- Stanford University
- Study ID
- NCT03826693
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Obsessive-Compulsive Disorder
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Nitrous Oxide — DRUGOCD participants in this arm will receive 50%oxygen/50% nitrous oxide admixture for 60 minutes.
- Nitrogen — DRUGOCD participants in this arm will receive 50%oxygen/50% nitrogen admixture for 60 minutes.
Study Details
This study investigates whether the commonly used and well-tolerated inhaled anesthetic nitrous oxide can rapidly improve symptoms of OCD.
Key Dates
- Start date
- Apr 17, 2021
- Status verified
- Aug 2025
- Primary completion
- Sep 30, 2026
- Completion
- Oct 31, 2027
Study Design
- Enrollment
- 45 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Experimental: Nitrous OxideOCD participants in this arm will receive 50%oxygen/50% nitrous oxide admixture for 60 minutes.
- Placebo Comparator: Control: NitrogenOCD participants in this arm will receive 50%oxygen/50% nitrogen admixture for 60 minutes.
Primary Outcome Measure
Improvement in the severity of OCD symptoms as measured by the Yale-Brown Obsessive Compulsive Scale (YBOCS) [ Time Frame: 1 week ]
Central Contacts
- Pavithra Mukunda, MS650-723-4095
- Sindu Menon, MBBS650-723-4095
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford University | Stanford | California | 94304 | Peter van Roessel, MD, PhD (PRINCIPAL_INVESTIGATOR) |
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