No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 85
Sex
Any
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Western University, Canada · Other
Who this trial is looking for
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This is a longitudinal study of the long-term health impact of cannabis smoking on the lungs. Participants will be followed over a period of 3 years, and impacts of cannabis smoking on the lungs will be measured with magnetic resonance imaging (MRI) using hyperpolarized xenon-129 gas, pulmonary function tests, exercise capacity, computed tomography images and questionnaires.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patient understands study procedures and is willing to participate in the study as indicated by the patient's signature
* Provision of written, informed consent prior to any study specific procedures
* Males and females aged 18-85
* Current or former cannabis smoker (medicinal…
Inclusion Criteria:
* Patient understands study procedures and is willing to participate in the study as indicated by the patient's signature
* Provision of written, informed consent prior to any study specific procedures
* Males and females aged 18-85
* Current or former cannabis smoker (medicinal or recreational) with or without concurrent tobacco smoking history
* Participant is able to perform reproducible pulmonary function testing (i.e. the 3 best acceptable spirograms have Forced Expiratory Volume in 1 second (FEV1) values that do not vary more than 150 millilitres)
* Participant is able to perform a breathhold for 16s
* FEV1 \> 25% predicted
* Forced Vital Capacity (FVC) \> 25% predicted and \>0.5 litres
Exclusion Criteria:
* Participant is, in the opinion of the investigator, mentally or legally incapacitated, preventing informed consent from being obtained, or cannot read or understand written material
* Participant is medically unstable in the opinion of the Principal Investigator
* Participant has a daytime room air oxygen saturation \<90% while lying supine
* Participant is unable to perform spirometry or plethysmography maneuvers
* Patient is pregnant at time of enrolment
* In the opinion of the investigator, patient suffers from any physical, psychological or other condition(s) that might prevent performance of the MRI, such as severe claustrophobia
* Patient has implanted mechanically, electrically or magnetically activated device or any metal in their body, which cannot be removed, including but not limited to pacemakers, neurostimulators, biostimulators, implanted insulin pumps, aneurysm clips, bioprosthesis, artificial limb, metallic fragment or foreign body, shunt, surgical staples (including clips or metallic sutures and/or ear implants) - at the discretion of the MRI Technologist.
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