Psychedelic Healing: Adjunct Therapy Harnessing Opened Malleability
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- Johns Hopkins University
- Study ID
- NCT07053917
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Chronic Stroke
- Hemiparesis After Stroke
- Hemiplegia Following Ischemic Stroke
- Hemiplegia and Hemiparesis
- Hemiplegia and/or Hemiparesis Following Stroke
- Intracerebral Haemorrhage
- Intracerebral Haemorrhage (ICH)
- Intracerebral Hemorrhage Basal Ganglia
- Ischemic Stroke
- Ischemic Stroke and Hemorrhagic Stroke
- Middle Cerebral Artery Stroke
- Stroke
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Psilocybin (Usona Institute) — DRUGParticipants will receive psilocybin to test its safety. Secondary outcomes will assess recovery from post-stroke deficits.
Study Details
The main purpose of the current studies is to evaluate the safety and tolerability of psilocybin in patients with chronic stroke.
Key Dates
- Start date
- Feb 9, 2026
- Status verified
- Feb 2026
- Primary completion
- Feb 28, 2027
- Completion
- Mar 31, 2027
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: 25 mg of psilocybinParticipants will receive 25 mg of psilocybin
- Experimental: 12.5 mg + 12.5 mg of psilocybinParticipants will receive 12.5 mg of psilocybin followed by another 12.5 mg of psilocybin 2 hours after the first dose.
Primary Outcome Measure
Stability of systolic and diastolic blood pressure (mmHg) [ Time Frame: up to 24 hours post-psilocybin administration ]
Central Contacts
- Steven R Zeiler, M.D., Ph.D.303-520-7404
- Victor C Urrutia, M.D.443-254-6435
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Johns Hopkins | Baltimore | Maryland | 21287 | - |
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