Psilocybin AsSisted pSychotherapy for the treatmENt of Gambling disordER : a Pilot Study
Starting soon · Phase 2
Conditions studied: Gambling Disorder
In brief
The PASSENGER project aims to conduct a pilot feasibility study of the implementation of a randomized clinical trial on psilocybin-assisted psychotherapy for the treatment of gambling disorder. Feasibility will be assessed by estimating the ability to retain participants until the end of the protocol. Other objectives of the study will be to generate preliminary efficacy data, identify clinical factors potentially associated with the intensity of the psychedelic experience (which determines the expected therapeutic effect), and conduct a preliminary assessment of the safety of the treatment under study.
Key facts
- Study ID
- NCT07391332
- Run by
- Nantes University Hospital
- People needed
- 30
- Starts
- 2026-04-01
- Expected to finish
- 2029-01-01
- Last updated by the study team
- 2026-02-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Men and women aged 18 years or older
- With a confirmed diagnosis of current gambling disorder (diagnostic criteria according to DSM-5), regardless of severity.
- Able to complete self-assessment questionnaires
- Willing to start addiction treatment, or for whom treatment already undertaken is not sufficient
- Willing to undergo a blood test and ECG
- Written and oral comprehension of French
- Having signed an informed consent form before any procedure under study
- Affiliated with a French social security system
- Women of childbearing age with a negative pregnancy test and highly effective contraception (according to version 1.2 of March 2024 of the CTCG recommendations in Appendix 7)
- Men of childbearing age using effective contraception (according to version 1.2 of March 2024 of the CTCG recommendations).
- Negative result on urinary toxicology screening
- In the case of psychotropic treatment (excluding nicotine replacement therapy): stabilization of dosage or initiation for more than 1 month.
You may not qualify if…
- Medical conditions that would prevent safe participation in the trial (epilepsy, significantly impaired liver function (TP<50%), significantly impaired kidney function (GFR<90 mL/min), coronary artery disease, history of arrhythmia, heart failure, uncontrolled hypertension, history of stroke, severe asthma, hyperthyroidism, narrow-angle glaucoma, symptomatic prostatic hypertrophy, or bladder neck obstruction).
- Serious ECG abnormalities (including QTc prolongation = corrected QT)
- Current or past psychotic or bipolar disorder
- Other unstable psychiatric disorder
- Family history (first-degree relatives) of psychotic disorder or type 1 bipolar disorder
- Current high risk of suicide (according to the MINI 5.0 suicide risk module)
- History of hallucinogen use disorder or any use in the past year
- Current alcohol use disorder with a history of withdrawal symptoms
- Extreme thinness (BMI < 16.5) or obesity (BMI > 30)
- Major cognitive impairment (Mini-Mental State Examination score < 26)
- Allergy or hypersensitivity to psilocybin or any of the excipients contained in the investigational drug
- Taking UGT1A9, UGT1A10, ALDH, or ADH inhibitors
- Pregnancy or breastfeeding
- Current protective measures (guardianship and legal protection)
- Participation in another interventional research protocol involving another psychotherapeutic or pharmacological intervention that may have an impact on clinical progression
Where it is running
- Nantes University Hospital — Nantes, France
Full record on ClinicalTrials.gov
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