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| ID | Type | Description | Link |
|---|---|---|---|
| NFL-CBD-01 | Other Identifier | URegina |
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| Name | Class |
|---|---|
| National Football League | OTHER |
| My Next Health Inc. | UNKNOWN |
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The goal of this open-label, placebo-controlled, dosage escalation study is to learn about the safety of a Cannabis/Hemp Isolate Extract in normal healthy adults engaged in elite contact sport competition.
The main question it aims to answer is:
• Are cannabis/hemp-based products with high CBD safe, well-tolerated and without adverse physiological and psychological dysfunction, when administered on a daily basis?
Participants will:
This research project will be a Phase I clinical trial to test the safety, efficacy and tolerability of the drug formulation. Specifically, the investigators will use a dose escalation study with all participants taking a placebo before starting the CBD regimen. This study is designed to investigate anti-inflammatory and neuroprotection of the CBD formulation to determine whether it can be used on a daily basis safely during the periods of intensive exercise (resistance) training during the off-season prior to competition.
The primary research hypothesis is that cannabis/hemp-based products with high CBD are safe, well-tolerated and do not cause adverse physiological and psychological dysfunction when administered on a daily basis. Specifically, the investigators will investigate the pharmacokinetic, physiological, and psychological effects of CBD. The investigators hypothesize that the CBD formulations will be non-intoxicating (non-psychotropic), safe, well-tolerated and do not cause adverse physiological or psychological dysfunction.
Secondary research hypotheses for this clinical trial:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Dose Escalation | Experimental | When participants start the CBD, they will be started on a low dose of CBD, beginning at 5 mg CBD/kg body mass, and then increased by 5 mg/kg every 2-weeks until 30 mg CBD/kg body mass is taken. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cannabis/Hemp Isolate Extract | Drug | Formulation: CBD (99%; 0.1% THC isolate) |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in cerebrovascular and cardiovascular physiology | Monitor the participant's cerebrovascular and cardiovascular physiology before and after the dosage regimen | Every 15 days from Day 0 to Day 104 |
| Incidence of potential harmful side effects | Follow the participants enrolled in these studies at set intervals to monitor for potential harmful side effects of the high CBD cannabis/hemp extract. This will include bloodwork to assess for possible hematopoietic, renal or hepatic dysfunction, and pharmacokinetic and pharmacodynamic analysis of the dose escalation protocol | Every 15 days from Day 0 to Day 104 |
| Measure | Description | Time Frame |
|---|---|---|
| Assessment of GABAergic activity | Assess the inhibitory neurotransmitter δ-aminobutyric acid (GABAergic activity) | Every 15 days from Day 0 to Day 104 |
| Change in pain intensity | Pain Behaviour Measurement system (PBM) scale |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Patrick Neary | University of Regina | Study Director |
| Payam Dehghani, | Saskatchewan Health Authority - Regina Area | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Regina | Regina | Saskatchewan | S4S 0A2 | Canada | ||
| Pasqua Hospital |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 39266961 | Derived | Neary JP, Singh J, Alcorn J, Laprairie RB, Dehghani P, Mang CS, Bjornson BH, Hadjistavropoulos T, Bardutz HA, Bhagaloo L, Walsh Z, Szafron M, Dorsch KD, Thompson ES. Pharmacological and physiological effects of cannabidiol: a dose escalation, placebo washout study protocol. BMC Neurol. 2024 Sep 12;24(1):340. doi: 10.1186/s12883-024-03847-1. |
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All participants will receive placebo at Day 0. CBD 5 mg/kg will begin Day 15. CBD 10 mg/kg will begin Day 30. CBD 15 mg/kg will begin Day 45. CBD 20 mg/kg will begin Day 60. CBD 25 mg/kg will begin Day75. CBD 30 mg/kg will begin Day 90.
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| Every 15 days from Day 0 to Day 104 |
| Cerebral blood flow (transcranial Doppler) | Assessment of cerebral hemodynamic activity | Every 15 days from Day 0 to Day 104 |
| Cerebral oxygenation (near infrared spectroscopy) | Assessment of cerebral hemodynamic activity | Every 15 days from Day 0 to Day 104 |
| Change in QoL | Assess quality of life (QOL) in study participants by scores on health questionnaires and medication use | up to day 104 |
| Incidence of AEs | Assess adverse events (AEs) in study participants by looking at sleepiness/lethargy, irritability, nausea/vomiting and diarrhea | Through study completion, From Day 0 to Day 104 |
| Regina |
| Saskatchewan |
| S4T 7T1 |
| Canada |