Psilocybin With Intracranial Neural Sensing
Part of paid clinical trials in San Francisco, California.
- Sponsor
- Joshua Woolley, MD, PhD
- Study ID
- NCT06919640
- Phase
- PHASE1
- Status
- Enrolling By Invitation
Conditions
- Chronic Pain
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Psilocybin — DRUG10mg oral psilocybin
Study Details
This is an open-label, single-arm, pilot study exploring the neural, sensory, and cognitive effects of a single, medium dose of psilocybin in patients with chronic pain who already have implanted sensing-capable deep brain stimulation (DBS) devices. Outcomes include multi-site neural recording from previously placed ambulatory sensing-capable DBS devices, quantitative sensory and cognitive testing, and self-reports of pain. We hypothesize that psilocybin will change functional connectivity, decrease clinical and task-based pain reports, and improve cognitive functions.
Key Dates
- Start date
- Jun 1, 2025
- Status verified
- Apr 2025
- Primary completion
- Apr 30, 2028
- Completion
- Apr 30, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- OTHER
Arms
- Experimental: 10mg oral psilocybin
Primary Outcome Measure
Changes in neural functional connectivity [ Time Frame: Drug administration to 90 days following ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, San Francisco | San Francisco | California | 94143 | - |
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