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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04693884
Other study ID # UOG-HPL-CAN (REB# 18-11-013)
Secondary ID
Status Active, not recruiting
Phase Early Phase 1
First received
Last updated
Start date September 1, 2021
Est. completion date December 2023

Study information

Verified date November 2023
Source University of Guelph
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This two-phase project seeks to examine the cardiovascular response to consumption of cannabis variants of different cannabinoid composition through different methods (smoking vs. vaporizing), at rest and during aerobic exercise. Multiple measures that have been shown to predict risk factors for chronic-disease and negative health outcomes will be assessed following cannabis consumption at rest or in combination with exercise. These techniques will examine arterial stiffness, vascular function, and cardiac function. In phase I and II, subjects will visit the lab on 6 different occasions; with 1 visit acting as an introductory visit, 1 as an exercise control visit, 2 as resting cannabis visits, and 2 as cannabis + exercise visits. Cannabis used in phase I of this study will consist of approximately 10% THC. On all visits, pulse wave velocity, flow mediated dilation, and echocardiography measures will be performed following cannabis consumption by smoking or vaporizing, and cannabis consumption by smoking or vaporizing followed by 20 minutes of exercise on a cycle ergometer. Phase II of the study will implore a similar design. In favor of altering method of consumption, in all visits cannabis will be consumed by vaporization and will be either a high cannabidiol (CBD: (~10%)) and low delta-9-tetrahydrocannabinol (THC: (<1%)), or a high THC (~10%) and low CBD (<1%) variant.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 45 Years
Eligibility Inclusion Criteria: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Male or female, aged 19-45yr 4. In good general health as evidenced by medical history and free of chronic disease 5. Must be experienced with cannabis use. This requires recreational cannabis use of a minimum of once per week in the past 30 days as confirmed by urine test 6. Experience consuming cannabis recreationally by vaping dried cannabis Exclusion Criteria: 1. Deemed unfit to exercise by the PARQ+. 2. Current or past diagnoses of substance abuse disorder 3. Failure of recreational substance urine screening test 4. Current, past, or strong family history of psychosis, or has previously experienced a cannabis-related psychotic episode 5. Current or past diagnoses of cannabis use disorder 6. Current or past diagnoses of any mood or anxiety disorder 7. Identified ECG abnormalities 8. Systolic blood pressure exceeding 160mmHg 9. Diastolic blood pressure exceeding 90mmHg 10. Resting heart rate exceeding 100bpm, or lower than 40bpm 11. Diagnosed with respiratory disease 12. Diagnosed with cardiovascular disease 13. Diagnosed with liver disease 14. Diagnosed with kidney disease 15. Is Pregnant or planning to be pregnant 16. Currently taking prescription medication (excluding contraceptive medication) 17. Is a cigarette smoker

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Cannabis
Cannabis of (~10% THC concentration <1% CBD concentration) will be smoked.
Cannabis
Cannabis of (~10% THC concentration <1% CBD concentration) will be vaporized.
Cannabis
Cannabis of (~10% CBD concentration <1% THC concentration) will be smoked.
Cannabis
Cannabis of (~10% CBD concentration <1% THC concentration) will be vaporized.

Locations

Country Name City State
Canada University of Guelph Guelph Ontario

Sponsors (1)

Lead Sponsor Collaborator
Jamie Burr

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Aortic Stiffness From Baseline Following Cannabis Consumption Assessed via carotid-femoral pulse wave velocity (PWV) Baseline, Post-Intervention (<2 Hours)
Primary Change in Brachial Artery Vascular Function From Baseline Following Cannabis Consumption Assessed via brachial artery flow mediated dilation (FMD) Baseline, Post-Intervention (<2 Hours)
Primary Change in Sympathetic Nervous System Activity From Baseline Following Cannabis Consumption Assessed via microneurographic recordings of the peroneal nerve Baseline, Post-Intervention (<2 Hours)
Primary Change in Cardiac Function From Baseline Following Cannabis Consumption Measured by echocardiography Baseline, Post-Intervention (<2 Hours)
Secondary Exercise Capacity Assessed by maximal average power attainable during 20 minutes of continuous cycling exercise Baseline, Post-Intervention (<2 Hours)
Secondary Heart Rate Measured at rest and during exercise Baseline, Post-Intervention (<2 Hours)
Secondary Systolic Blood Pressure Measured at rest and during exercise Baseline, Post-Intervention (<2 Hours)
Secondary Diastolic Blood Pressure Measured at rest and during exercise Baseline, Post-Intervention (<2 Hours)
Secondary Perceived Exertion Measured during exercise Baseline, Post-Intervention (<2 Hours)
Secondary Oxygen Consumption Measure of metabolic activity Baseline, Post-Intervention (<2 Hours)
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