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Taking peopleEarly phase 1

Trauma-informed Psilocybin Assisted Psychotherapy (TiPAP) for PTSD

Key facts

Who runs it
Tel-Aviv Sourasky Medical Center
Where
Israel1 site in 1 countryChoose a country to see its sites
Trial code
Status
Recruiting
Phase
Early phase 1
People taking part
13 people, planned
Started
22 Jul 2025
Expected to end
31 Dec 2026
Type of study
Interventional
Treatments tested
  • Psilocybin (drug)
  • Trauma-Focused Psychotherapy
Record updated
30 July 2026

Who can take part

Age
21 years to 65 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 26 criteriaShow less

Who can take part

  • Age 21-65 years
  • Diagnosis of post-traumatic stress disorder (PTSD) according to DSM-5 criteria, as assessed by CAPS-5
  • At least 1 year since the traumatic event
  • Moderate or greater PTSD severity (CAPS-5 score ≥ 25)
  • Ability to provide written informed consent
  • Ability to read, write, speak, and understand Hebrew
  • Prior trauma-focused psychotherapy
  • Medically healthy at screening, as determined by a study physician, including:; No exclusionary medical conditions; Resting blood pressure between 90/60 and 150/90 mmHg and heart rate between 45-100 bpm; Normal laboratory results (including liver function, renal function, and electrolytes)

Who cannot take part

  • Use of psychedelic substances within 3 months before enrollment
  • Pregnancy, breastfeeding, or positive pregnancy/drug test (excluding cannabis) on the day of dosing
  • Use of medications contraindicated with psilocybin
  • Changes in psychiatric medication (dose or type) within one month before enrollment
  • Current or past diagnosis of psychotic disorders, bipolar disorder, schizoaffective disorder, dissociative identity disorder, or borderline personality disorder (as assessed by MINI or SCID-5-SPQ)
  • First-degree relative with a history of a psychotic disorder
  • History of antidepressant-induced mania or hypomania
  • Substance use disorder (excluding nicotine and caffeine); mild-to-moderate alcohol or cannabis use may be permitted under monitoring and PI approval
  • History of adverse psychological reaction to psychedelics requiring hospitalization
  • Significant cardiovascular disease, including ischemic heart disease, uncontrolled hypertension, arrhythmia, or heart failure (NYHA class ≥3)
  • Dementia or suspected cognitive impairment
  • Current psychotic features
  • Significant suicidal risk as assessed by the Columbia Suicide Severity Rating Scale (C-SSRS), including active suicidal ideation with intent or plan, or suicidal behavior within the past 6 months
  • Participation in a clinical trial involving administration of a psychedelic substance within the past 12 months
  • Traumatic brain injury with loss of consciousness >24 hours or post-traumatic amnesia >7 days (unless cleared by neurological evaluation)
  • BMI <18 or >33
  • Abnormal liver or renal function tests
  • Needle phobia or inability to undergo blood testing

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 21 and 65 years old?

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

This is an open-label pilot study designed to evaluate the safety, tolerability, and preliminary clinical effects of psilocybin-enhanced trauma-focused psychotherapy in individuals with post-traumatic stress disorder (PTSD).

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Participants will receive a structured therapeutic protocol that includes preparatory sessions, two psilocybin administration sessions (15 mg followed by 25 mg), and integration sessions based on a trauma-focused therapeutic approach.

The primary objective of the study is to assess the safety and tolerability of psilocybin administration in this clinical population. Secondary objectives include evaluating changes in PTSD symptom severity, as measured by the Clinician-Administered PTSD Scale (CAPS-5), at 30 days following treatment.

This pilot study will include 13 participants and is intended to inform the feasibility and design of a subsequent randomized controlled trial.

The group in the trial

  • Psilocybin-Assisted Trauma-Focused PsychotherapyTreatment being tested

    Participants receive a structured clinical intervention combining preparatory psychotherapy sessions, two psilocybin dosing sessions (15 mg and 25 mg), and integration psychotherapy sessions within a trauma-focused therapeutic framework.

    Treatment: Psilocybin (drug) and Trauma-Focused Psychotherapy

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Trauma-informed Psilocybin Assisted Psychotherapy (TiPAP) for Post-Traumatic Stress Disorder
Fit questions
Built from NCT07737054, who can take part
Record updated
30 July 2026