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NOT YET RECRUITING
NCT05320367
PHASE1/PHASE2

A Study of Inhaled Cannabidiol in Healthy Occasional Cannabis Users

Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)

View on ClinicalTrials.gov

Summary

The purposes of this study are 1) to determine if the administration of different low doses of CBD (5 mg, 20 mg, 50 mg and 100 mg) result in detectable subjective pleasant drug effect compared to placebo and 2) to qualitatively explore whether low dose CBD is associated with effects that are not detected with the available research tools.

Official title: A Randomized, Triple Blinded Cross-over Placebo Controlled Study of Effects of Inhaled Cannabidiol in Healthy Occasional Cannabis Users

Key Details

Gender

All

Age Range

21 Years - 49 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2026-09

Completion Date

2027-12

Last Updated

2025-12-22

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

Cannabis, placebo

Eligible participant will be randomize 1:1:1:1:1 to receive placebo, CBD (5mg, 20mg, 50mg and 100mg). Only one research product will be inhaled for each visit. The sequence will depend on the assigned randomization group.