Informations générales
  • Catégorie de maladie Autre (BASEC)
  • Study Phase N/A (ICTRP)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Berne, Luzern
    (BASEC)
  • Responsable de l'étude Prof. Dr. med. Reto Auer reto.auer@biham.unibe.ch (BASEC)
  • Source(s) de données BASEC: Importé de 08.07.2025 ICTRP: Importé de 13.12.2024
  • Date de mise à jour 08.07.2025 12:41
HumRes63386 | SNCTP000005702 | BASEC2022-00733 | NCT06120855

A randomized controlled pilot study on the regulated sale of cannabis in pharmacies

  • Catégorie de maladie Autre (BASEC)
  • Study Phase N/A (ICTRP)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Berne, Luzern
    (BASEC)
  • Responsable de l'étude Prof. Dr. med. Reto Auer reto.auer@biham.unibe.ch (BASEC)
  • Source(s) de données BASEC: Importé de 08.07.2025 ICTRP: Importé de 13.12.2024
  • Date de mise à jour 08.07.2025 12:41

Résumé de l'étude

Cannabis is the most commonly consumed illegal substance in Switzerland. The regulation of cannabis sales has been discussed for a long time to curb the black market and its negative aspects. However, current knowledge about the consequences of regulation remains severely limited. Many cannabis consumers smoke cannabis and often also tobacco. Smoking is one of the biggest public health problems and is considered the main risk factor for many diseases. With a combination of regulated distribution and appropriate education about less harmful alternatives to smoking (e.g., E-Joints), this situation could be improved. The main objective of this study is to evaluate how such an offer (regulated cannabis distribution plus education/support for problematic substance use) affects adults who already regularly consume cannabis. Primarily, consumption behavior, especially the switch from smoking to alternative consumption methods, will be evaluated. Additionally, health and social impacts will be analyzed. Participants will be randomly assigned to one of two groups. One group can purchase cannabis products from the beginning in pharmacies, while the other group is only allowed to do so after 6 months. Both groups have regular study visits for data collection.

(BASEC)

Intervention étudiée

Participants can purchase cannabis in various forms of consumption at the pharmacy. They are encouraged to switch from smoking to alternative methods such as vaping, vaporizing, or oral intake. At the same time, information about health and cannabis consumption as well as support for quitting smoking and for problematic drug or alcohol use is provided. The study is subject to strict quality criteria for the production and storage of regulated cannabis products.

(BASEC)

Maladie en cours d'investigation

This study examines individuals who consume cannabis for non-medical purposes in their leisure time.

(BASEC)

Critères de participation
- regular cannabis consumption - at least 18 years old - residence in the canton where the study is conducted (BASEC)

Critères d'exclusion
- pregnancy or breastfeeding - prescription to obtain medical cannabis - severe psychosis or suicidal thoughts (BASEC)

Lieu de l’étude

Berne, Luzern

(BASEC)

Switzerland (ICTRP)

Sponsor

Universität Bern Berner Institut für Hausarztmedizin Abteilung Substanzkonsum

(BASEC)

Contact pour plus d'informations sur l'étude

Personne de contact en Suisse

Prof. Dr. med. Reto Auer

031 684 58 79

reto.auer@biham.unibe.ch

Universität Bern Berner Institut für Hausarztmedizin Abteilung Substanzkonsum

(BASEC)

Informations générales

Institute of Primary Health Care (BIHAM), Faculty of Medicine, University of Bern,

+41 31 684 58 79

reto.auer@biham.unibe.ch

(ICTRP)

Informations scientifiques

Institute of Primary Health Care (BIHAM), Faculty of Medicine, University of Bern,

+41 31 684 58 79

reto.auer@biham.unibe.ch

(ICTRP)

Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)

Commission cantonale d'éthique de Berne

(BASEC)

Date d'approbation du comité d'éthique

05.09.2023

(BASEC)


Identifiant de l'essai ICTRP
NCT06120855 (ICTRP)

Titre officiel (approuvé par le comité d'éthique)
The Safer Cannabis – Research In Pharmacies randomized controlled Trial (SCRIPT) (BASEC)

Titre académique
The Safer Cannabis - Research In Pharmacies Randomized Controlled Trial (SCRIPT) (ICTRP)

Titre public
Study on Regulated Cannabis Sales in Pharmacies (ICTRP)

Maladie en cours d'investigation
Marijuana Smoking;Cannabis;Cannabis Use (ICTRP)

Intervention étudiée
Drug: Regulated cannabis from authorized pharmacies;Drug: Cannabis from the illicit market (ICTRP)

Type d'essai
Interventional (ICTRP)

Plan de l'étude
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label). (ICTRP)

Critères d'inclusion/exclusion
Gender: All
Maximum age: N/A
Minimum age: 18 Years
Inclusion Criteria:

- At least 18 years old (validated with valid identification document)

- Written informed consent

- Regular cannabis user: Self-reported cannabis use at least once a month over the
last 6 months and verified cannabis exposure based on urine analysis at baseline

- Resident status in the canton of Bern (for cannabis purchase in the cities of Bern
or Biel) or in the city of Lucerne (for cannabis purchase in the city of Lucerne)
(validated with registration confirmation from the municipality or confirmation of
the residential address)

Exclusion Criteria:

- Pregnant women (pregnancy test based on urine sample)

- Breastfeeding women (self-reported)

- People with a prescription for medical cannabis (self-reported)

- People currently in psychiatric inpatient treatment (self-reported)

- People with current, severe psychosis (self-reported and confirmed by study
nurse/study physician)

- People with current, severe suicidal thoughts (self-reported and confirmed by study
nurse/study physician)

- Inability to follow the procedures of the study due to severe cognitive impairment
or language problems

- People who cannot attend the baseline study visit in-person

- People planning to move out of the canton of residence within 6 months of entering
the trial.

- People who are participating or have participated (inclusion date up to one year
ago) in another cannabis pilot trial which allows to buy regulated cannabis
(validated by matching untraceable codes between studies witch the same catchment
area). (ICTRP)

non disponible

Critères d'évaluation principaux et secondaires
Self-reported cannabis and tobacco smoking abstinence in the 7 days prior to the 6-months follow-up visit, validated by carbon monoxide (CO) in exhaled air (ICTRP)

Self-reported reported 7-days point prevalence abstinence from cannabis and tobacco smoking at 6 months follow-up, without validation by CO in exhaled air.;Shift from smoking to safer, alternative delivery methods of cannabis and, if applicable, tobacco.;Concentration of toxicants in urine;Type of cannabis sold per participant in pharmacies;Amount of cannabis sold per participant in pharmacies;Self-reported cannabis purchase on the illicit market;Self-reported frequency of use;Concentration of THC and CBD in cannabis bought on the illicit market;Concentration of contaminants in cannabis bought on the illicit market;Severity of generalised anxiety disorder;Attention Deficit Hyperactivity Disorder (ADHD) symptoms in adults;Severity of depression;Number of psychotic symptoms;Somatic health;Impact of COPD;Severity of dyspnea;COPD exacerbation assessment;Quality of life (health-related);Perception of stress;Cannabis use and purchase behavior;Cannabis use disorder;Consumption motives;Consumption competence;Consumption risk perception;Nicotine/tobacco use behavior;Exposure to second-hand smoke;Alcohol consumption behavior;Drug consumption behavior;Medication use behavior;Treatment/Counseling Experience;Use of health and social services;Body mass index;Blood pressure;Waist-to-hip ratio;Number of safety events;Inflammation-related protein biomarkers;Blood biomarker for alcohol and cannabis exposure (ICTRP)

Date d'enregistrement
19.10.2023 (ICTRP)

Inclusion du premier participant
non disponible

Sponsors secondaires
Universit?t Luzern (ICTRP)

Contacts supplémentaires
Reto Auer, Prof.;Reto Auer, Prof., reto.auer@unibe.ch, +41 31 684 58 79, Institute of Primary Health Care (BIHAM), Faculty of Medicine, University of Bern, (ICTRP)

ID secondaires
SCRIPT (ICTRP)

Résultats-Données individuelles des participants
non disponible

Informations complémentaires sur l'essai
https://clinicaltrials.gov/ct2/show/NCT06120855 (ICTRP)

Résultats de l'essai

Résumé des résultats

non disponible

Lien vers les résultats dans le registre primaire

non disponible