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Cannabis Edibles and Simulated Driving

C

Center for Addiction and Mental Health (CAMH)

Status

Completed

Conditions

Cannabis
Driving Under the Influence

Treatments

Drug: Cannabis - High Dose (20 mg)
Drug: Cannabis - Low Dose (2 mg)
Drug: Cannabis - Placebo Dose (0 mg)
Drug: Cannabis - Medium Dose (10 mg)

Study type

Interventional

Funder types

Other

Identifiers

NCT06595576
074-2020

Details and patient eligibility

About

The goal of this human laboratory experiment is to determine the acute and residual effects of a range of doses of orally administered cannabis edibles on driving simulator performance in people who use cannabis recreationally. Four conditions will be tested: placebo, low dose, medium dose and high dose. Driving performance will be tested objectively using a driving simulator during a number of pre-programmed driving scenarios. The investigators will test the hypothesis that driving performance on a high-fidelity driving simulator will decrease with increasing doses of cannabis. Secondary objectives will:

  • Determine the acute and residual (24 hour) cognitive, behavioural, and physiological effects of a range of doses of orally administered cannabis edibles on subjective effects, cognitive tests, verbal memory, and mood.
  • Examine how the concentration of THC in blood and oral fluids correlates with driving simulator performance, as well as cognitive, behavioural, and physiological measures. Cannabinoid levels in blood, urine and oral fluids will be measured at baseline and over a 5 hour period following drug exposure. The investigators will examine the relationship between cannabinoid levels and performance measures in this time frame.
  • Explore potential biomarkers of acute exposure to cannabis edibles by analyzing the following: circulating cell-free mtDNA (ccf-mtDNA), endocannabinoids, and metabolic biomarkers.

Enrollment

52 patients

Sex

All

Ages

19 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Provides written and informed consent
  • Stated the willingness to comply with all study procedures
  • Recreational use of oral, vaped, smoked or edible cannabis (at least one day/week) and cannabis edibles (at least one day/month) confirmed by self-report and urine screening (i.e., positive THC result in point-of-care screening or Clinical Laboratory assay)
  • Males and females aged 19 to 45 years
  • Has held a class G license (or equivalent from another jurisdiction) for at least 12 months
  • Willing to abstain from using cannabis for 72 hours prior to each practice or test session
  • Willing to abstain from alcohol for 48 hours prior to each practice or test session, and to abstain from all other drugs not medically required for the duration of the study (beginning 48 hours prior to the practice session)
  • Lives within a radius that costs less than about $60 per taxi ride
  • Able to consume the quantity of candies and drive the driving simulator as determined by a practice session
  • A negative urine pregnancy test for those with childbearing potential
  • Use of appropriate contraception for those with childbearing potential

Exclusion criteria

  • Diagnosis of severe medical or psychiatric condition (e.g., diagnosis of a severe mood or anxiety disorder, based on self-report
  • Meets criteria for current or lifetime alcohol or other substance use disorder (DSM-5), except tobacco use disorder and caffeine use disorder
  • Regular user of medication that may affect cognitive functioning and/or driver performance (e.g. ADHD medication, benzodiazepines, stimulants, opioids)
  • Regular user of illicit substances
  • Personal or family history of schizophrenia or other psychotic disorder
  • Pregnant, looking to become pregnant, or breastfeeding
  • Concomitant therapy with sedative-hypnotics or other psychoactive drugs
  • Severe laboratory abnormalities that could create safety issues based on the judgement of the Principal Investigator
  • Cardiovascular or cerebrovascular disease
  • Severe renal or liver disease
  • Participation in another clinical or non-therapeutic study in the past month

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

52 participants in 4 patient groups

Placebo Cannabis Edibles (0 mg THC)
Experimental group
Description:
Participants consume a placebo dose of cannabis edibles (0 mg THC).
Treatment:
Drug: Cannabis - Placebo Dose (0 mg)
Low Dose Cannabis Edibles (2 mg THC)
Experimental group
Description:
Participants consume a low dose of cannabis edibles (2 mg THC).
Treatment:
Drug: Cannabis - Low Dose (2 mg)
Medium Dose Cannabis Edibles (10 mg)
Experimental group
Description:
Participants consume a medium dose of cannabis edibles (10 mg THC).
Treatment:
Drug: Cannabis - Medium Dose (10 mg)
High Dose Cannabis Edibles (20 mg)
Experimental group
Description:
Participants consume a high dose of cannabis edibles (20 mg THC).
Treatment:
Drug: Cannabis - High Dose (20 mg)

Trial contacts and locations

1

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Central trial contact

Bernard Le Foll, MD, PhD; Madison Wright, PhD

Data sourced from clinicaltrials.gov

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