Stroke study: Psilocybin
Official title Psychedelic Healing: Adjunct Therapy Harnessing Opened Malleability
ClinicalTrials.gov ID: NCT07053917
What this study is testing
What is Psilocybin (Usona Institute)?
Psilocybin (Usona Institute) is an investigational medicine, being studied as a potential treatment for stroke.
Plain-language explanation of the investigational treatment. It is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- The study aims to find out if psilocybin is safe and well‑tolerated in patients with chronic stroke.
- Who it's for
- Adults who have experienced a stroke and are in the chronic phase.
- What's involved
- Participants will receive a dose of psilocybin and be monitored with medical visits and tests to check for side effects.
- Phase 1: an early, usually small safety study
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- 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...
- Are willing to follow restrictions and guidelines concerning medications, consumption of food, beverages, and nicotine the night before and just...
You likely can't join if
- selective serotonin reuptake inhibitor (SSRI)
- Serotonin-norepinephrine reuptake inhibitors (SNRI)
- Buproprion
- Valproic acid
- Zolpidem
- Trazodone
See the full eligibility 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...
- 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 treatment clinical trials during the duration of this study.
- selective serotonin reuptake inhibitor (SSRI)
- Serotonin-norepinephrine reuptake inhibitors (SNRI)
- Buproprion
- Valproic acid
- Zolpidem
- Trazodone
- Carbamazepine.
- tricyclic antidepressants
- Monoamine Oxidase Inhibitors
- 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.
- 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.
The study team makes the final eligibility decision.
Where it is enrolling
- Baltimore, Maryland, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
This study is enrolling now at Baltimore, Maryland, United States. Enter your location above to see the nearest enrolling site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.