Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:16 PM
Ignite Modification Date:
2026-03-26 @ 3:16 PM
NCT ID:
NCT07391332
Eligibility Criteria:
Inclusion Criteria:
* 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.
Exclusion Criteria:
* 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
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07391332
Study Brief:
Protocol Section:
NCT07391332