Recruiting
Phase 1
Phase 2

THC & CBD

Sponsor:

Centre hospitalier de l'Université de Montréal (CHUM)

Code:

NCT06099379

Conditions

Cannabis

THC

Eligibility Criteria

Sex: All

Age: 21 - 49

Healthy Volunteers: Accepted

Interventions

∆9-tetrahydrocannabinol

Study Details

Brief summary:

The purposes of this study are 1) to determine if CBD modulates THC-induced acute psychoactive effects at different CBD:THC ratios, compared with the control product (0:20, 20:20, 40:20, 80:20, 120:20) and 2) to determine if different doses of CBD modulate other THC induced behavioral effects, compared with the control product and 3)To explore qualitatively whether CBD modulates THC effects by mechanisms that are not detected with standard clinical research tools.

Conditions

Cannabis

THC

Study ID

NCT06099379

Start date

Jun 27, 2024

Status verified date

Dec, 2025

Completion date

Dec 31, 2026

Anticipated

Primary completion date

Jul 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 21 - 49

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Between 21 and 49 years of age, inclusively;
2. Have used cannabis at least once in their lifetime and have used cannabis three days or less in the 30 days prior to enrollment;
3. Be able to provide a signed informed consent;
4. Willing to comply with study procedures and requirements as per protocol;
5. Have a forced expiratory volume in first second (FEV) less than or equal to 90 %;
6. Able to communicate and understand English or French language;
7. For female participants:

a. No childbearing potential, defined as: i. postmenopausal (12 months of spontaneous amenorrhea and ≥ 45 years of age); or ii. Documented surgically sterilized (i.e., tubal ligation, hysterectomy, or bilateral oophorectomy); or b. For female of childbearing potential: i. Must have negative pregnancy test result at screening and at subsequent visits.

ii. AND have no pregnancy plan while on the study iii. AND must agree to use a medically accepted method of birth control throughout the study.

Exclusion criteria

Participants will be excluded if any of the following criteria are met:

1. Any disabling medical condition, as assessed by medical history, physical exam, vital signs and/or laboratory assessments that, in the opinion of the study physician, precludes safe participation in the study or the ability to provide fully informed consent;
2. Severe psychiatric condition (history of schizophrenia, schizoaffective disorder or bipolar disorder; current acute psychosis, mania or current suicidality based on the Mini International Neuropsychiatric Interview);
3. Any other disabling, unstable or acute mental condition that, in the opinion of the study physician, precludes safe participation in the study or ability to provide fully informed consent;
4. Known chronic liver disease or aspartate transaminase/alanine transaminase (AST/ALT) two times higher than upper limit of normal values at screening visit;
5. Blood pressure higher than 130/80 mmHg;
6. Kidney disorders;
7. Bleeding disorders;
8. Current moderate or severe DSM-5 substance use disorder (except nicotine) according to SCID-V;
9. Currently pregnant, breastfeeding or planning to become pregnant either at screening or while enrolled in the study;
10. Pending legal action or other reason that, in the opinion of the study physician, might prevent study completion;
11. Use of medication within 7 days of experimental sessions; which, in the opinion of the Investigator, may interact with cannabis.
12. Participation in clinical studies or undergoing other investigational procedure involving cannabis or cannabinoids administration within 30 days prior to randomization.
13. Resting heart rate over 100 beats per minute.
14. Current body mass index (BMI) over 29.9 kg/m2.
15. Any clinically significant electrocardiogram abnormalities at screening visit.

Study Design

Enrollment

100 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: CBD:THC Group 1

Group will receive four doses of CBD:THC ratio (20:20 mg, 40:20 mg, 80:20 mg and 120:20 mg) and a control product CBD:THC ratio (0:20 mg).

Group will attend a total of five study visits (one for each study product) with at least 1 week between each visit.

The order in which the study products will be administered depend on the randomization sequence.

experimental: CBD:THC Group 2

Group will receive four doses of CBD:THC ratio (20:20 mg, 40:20 mg, 80:20 mg and 120:20 mg) and a control product CBD:THC ratio (0:20 mg).

Group will attend a total of five study visits (one for each study product) with at least 1 week between each visit.

The order in which the study products will be administered depend on the randomization sequence.

experimental: CBD:THC Group 3

Group will receive four doses of CBD:THC ratio (20:20 mg, 40:20 mg, 80:20 mg and 120:20 mg) and a control product CBD:THC ratio (0:20 mg).

Group will attend a total of five study visits (one for each study product) with at least 1 week between each visit.

The order in which the study products will be administered depend on the randomization sequence.

experimental: CBD:THC Group 4

Group will receive four doses of CBD:THC ratio (20:20 mg, 40:20 mg, 80:20 mg and 120:20 mg) and a control product CBD:THC ratio (0:20 mg).

Group will attend a total of five study visits (one for each study product) with at least 1 week between each visit.

The order in which the study products will be administered depend on the randomization sequence.

experimental: CBD:THC Group 5

Group will receive four doses of CBD:THC ratio (20:20 mg, 40:20 mg, 80:20 mg and 120:20 mg) and a control product CBD:THC ratio (0:20 mg).

Group will attend a total of five study visits (one for each study product) with at least 1 week between each visit.

The order in which the study products will be administered depend on the randomization sequence.

Interventions

∆9-tetrahydrocannabinol

Phytocannabinoids from plant inflorescences (CBD and THC dominant) - inhaled

Primary outcome measure

  • Objective and subjective measures of cannabinoids effect [ Time Frame: Prior to the Product administration ,10 minutes and 80 minutes after inhalation ]

Central Contacts and Locations

Locations

Centre de recherche du Centre Hospitalier Universitaire de Montréal

Recruiting

Montreal, Quebec, Canada, H2X0A9

Contacts

Principal Investigator:

Didier Jutras-Aswad, MD

More Information

Sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Last update posted

Dec 22, 2025

Last verified

Dec, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Centre hospitalier de l'Université de Montréal (CHUM) on 2025-12-22.