Recruiting
Phase 1

Psilocybin

Sponsor:

Johns Hopkins University

Code:

NCT07053917

Conditions

Stroke

Chronic Stroke

Intracerebral Haemorrhage

Intracerebral Haemorrhage (ICH)

Intracerebral Hemorrhage Basal Ganglia

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Psilocybin (Usona Institute)

Study Details

Brief summary:

The main purpose of the current studies is to evaluate the safety and tolerability of psilocybin in patients with chronic stroke.

Conditions

Stroke

Chronic Stroke

Intracerebral Haemorrhage

Intracerebral Haemorrhage (ICH)

Intracerebral Hemorrhage Basal Ganglia

Study ID

NCT07053917

Start date

Feb 9, 2026

Status verified date

Feb, 2026

Completion date

Mar, 2027

Anticipated

Primary completion date

Feb, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Over age 18 years, inclusive.
  • Ischemic or hemorrhagic stroke confirmed by CT or MRI, at least 12 months prior to admission date
  • Ability to give informed consent and understand the tasks involved.
  • Agree that, for the study duration, will refrain from: (1) No new prescription medications during the time of the study without approval of the study team, (2) taking any herbal supplement (except with prior approval of the research team), (3) taking any nonprescription medications with the exception of: 1. non-steroidal anti-inflammatory drugs. 2. acetaminophen. 3. vitamins. 4. or other over-the-counter medications approved by the research team
  • Are willing to follow restrictions and guidelines concerning medications, consumption of food, beverages, and nicotine the night before and just prior to psilocybin administration.
  • Agree to have transportation other than driving themselves home or to where the participants are staying after the administration of psilocybin.
  • Are willing to be contacted via telephone for all necessary telephone contacts.
  • Must have a negative pregnancy test if able to bear children.
  • Must provide a contact (relative, spouse, close friend or other caregiver) who is willing and able to be reached by the investigators in the event of a participant becoming suicidal.
  • Must agree to inform the investigators within 48 hours of any new medical conditions and procedures.
  • Are proficient in speaking and reading English.
  • Agree to have all clinical visit sessions recorded to audio and video.
  • Agree to not participate in any other interventional clinical trials during the duration of this study.

Exclusion Criteria:

  • Taking one of the following medications in the 30 days prior to psilocybin administration:

1. selective serotonin reuptake inhibitor (SSRI)
2. Serotonin-norepinephrine reuptake inhibitors (SNRI)
3. Buproprion
4. Valproic acid
5. Zolpidem
6. Trazodone
7. Carbamazepine.
8. tricyclic antidepressants
9. Monoamine Oxidase Inhibitors
10. Mirtazapine

l. Lithium m. Buspirone n. Atypical antipsychotics o. Zolpidem p.Carbamazepine q. Clonazepam r. Gabapentin s. Lamotrigine t. Levetiracetam u. Phenobarbital v. Phenytoin w. Topiramate x. Valproic Acid y. Zonisamide
  • History of medically significant suicide attempt.
  • Evidence of acute cardiac dysfunction as evidenced by either elevated troponin or EKG changes within 48 hours of administration.
  • Systolic blood pressure that is greater than 150 mmHg systolic on > 2 readings during the 7-day monitoring period AND blood pressure medication management has been assured.
  • Diastolic blood pressure that is greater than 100 mmHg systolic on > 2 readings during the 7-day monitoring period AND blood pressure medication management has been assured.
  • Systolic blood pressure is less than 90 mmHg systolic on > 2 readings during the 7-day monitoring period after blood pressure medication management has been assured.
  • Diastolic blood pressure is less than 30 mmHg systolic on > 2 readings during the 7-day monitoring period after blood pressure medication management has been assured.
  • Systolic blood pressure exceeds 160 mmHg or is less than 90 mmHg immediately prior to administration of psilocybin; patients are allowed to be on anti-hypertensives.
  • Diastolic blood pressure exceeds 100 mmHg or is less than 30 mmHg immediately prior to administration of psilocybin; patients are allowed to be on anti-hypertensives.
  • Cognitive impairment that, in the estimation of the study team, would preclude the use of the MindPod Dolphin.
  • History of physical or neurological condition that interferes with study procedures or assessment of motor function (e.g. severe arthritis, severe neuropathy, Parkinson's disease).
  • Social and/or personal circumstances that interfere with ability to perform follow up assessments.
  • Are pregnant or nursing.
  • Weigh less than 48 kg.
  • Are not able to give adequate informed consent.
  • Are actively abusing opioids, cocaine, Phencyclidine (PCP), amphetamines, or alcohol.
  • Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders (SCID-5) criteria for moderate or severe substance use disorder
  • Diagnosis of schizophrenia, history of prior psychosis, anxiety requiring hospitalization, or Type 1 bipolar.
  • Hypernatremia
  • Hypokalemia (but can have received repletion during the prior 24 hours)
  • Hyperkalemia
  • Glomerular filtration rate of < 30 ml/min
  • Elevated of white blood cell count
  • Hemoglobin < 7 g/dl
  • Platelet count < 100,000 g/dl
  • Acute cardiac dysfunction demonstrated by either troponin elevation (chronic elevation is acceptable), or EKG changes suggestive of acute coronary syndrome.
  • Active suicidal ideation as assess by the C-SSRS.

Study Design

Enrollment

20 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: 25 mg of psilocybin

Participants will receive 25 mg of psilocybin

experimental: 12.5 mg + 12.5 mg of psilocybin

Participants will receive 12.5 mg of psilocybin followed by another 12.5 mg of psilocybin 2 hours after the first dose.

Interventions

Psilocybin (Usona Institute)

Participants will receive psilocybin to test its safety. Secondary outcomes will assess recovery from post-stroke deficits.

Primary outcome measure

  • Stability of systolic and diastolic blood pressure (mmHg) [ Time Frame: up to 24 hours post-psilocybin administration ]

Central Contacts and Locations

Central contacts

Steven R Zeiler, M.D., Ph.D.

303-520-7404sz@jhmi.edu

Victor C Urrutia, M.D.

443-254-6435

Locations

Johns Hopkins

Recruiting

Baltimore, Maryland, United States, 21287

More Information

Sponsor

Johns Hopkins University

Last update posted

Feb 13, 2026

Last verified

Feb, 2026

Keywords

  • psychedelic
  • stroke
  • chronic stroke
  • intracerebral hemorrhage
  • stroke recovery
  • motor recovery
  • poststroke recovery
  • poststroke motor recovery
  • hemiparesis recovery
  • psychedelic safety

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-27. This information was provided to ClinicalTrials.gov by Johns Hopkins University on 2026-02-13. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.