St. Joseph's Healthcare Hamilton
Hamilton, Ontario, L8S 4A6, Canada
NCT Number: NCT05742724
POT-GFR-PK is a single dose pharmacokinetic study oral tetrahydrocannabinol (THC) and cannabidiol (CBD) in healthy adult controls and individuals with chronic kidney disease including those treated with in-center hemodialysis.
This study is active but is not currently recruiting participants.
25 year and older
All sexes
Interventional
Phase 1
Hamilton, Ontario, L8S 4A6, Canada
Adults aged greater than 25 years including 6 with eGFR>60ml/min/1.73m2, 6 eGFR 30-59ml/min/1.73m2, 6 eGFR <30ml/min/1.73m2 (CKD Epidemiology Collaboration equation) and 6 receiving in-center hemodialysis at least 2x weekly via a tunnelled catheter will receive THC 0.1mg/kg and CBD 2mg/kg by mouth in the form of MediPharm Labs-001 (MPL-001) (50mg CBD/2mg THC per 1mL). In healthy controls and participants with chronic kidney disease, blood samples will be collected at t=0, 1, 2, 3, 3.5 and 4 hours post THC/CBD administration. In participants receiving in-center hemodialysis, blood samples will be collected at t=0, 1, 2, 3, 3.5 and 4 hours post THC/CBD administration and during hemodialysis at t=0, 60, 120, 180 minutes and 15 minutes prior to the end of hemodialysis (at a reduced pump speed with blood flow 50-100ml/min) and 60 minutes post-hemodialysis. A 24 hour urine will be collected in all participants except those receiving hemodialysis without any residual urine output. Dialysate samples will be collected at 1,2,3 hours during hemodialysis and at the end of hemodialysis. Blood samples will also be collected at 24 and 48 hours. Plasma, urine and dialysis cannabinoids (THC, CBD and their metabolites) will be quantified using Multisegment Injection-Capillary Electrophoresis-Mass Spectrometry.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Oral THC 0.1mg/kg and CBD 2.5mg/kg
Time frame: 48 hours
Maximum concentration (Cmax)
Time frame: 48 hours
Time to Cmax
Time frame: 48 hours
Last detection time
Time frame: 48 hours
Area under the curve
Time frame: 48 hours
Renal clearance
Time frame: 48 hours
Dialytic clearance
Time frame: 48 hours
Maximum concentration (Cmax)
Time frame: 48 hours
Time to Cmax
Time frame: 48 hours
Last detection time
Time frame: 48 hours
Area under the curve
Time frame: 48 hours
Renal clearance
Time frame: 48 hours
Dialytic clearance
Time frame: 48 hours
Maximum concentration (Cmax)
Time frame: 48 hours
Time to Cmax
Time frame: 48 hours
Last detection time
Time frame: 48 hours
Area under the curve
Time frame: 48 hours
Renal clearance
Time frame: 48 hours
Dialytic clearance
Time frame: 48 hours
Weakness, fatigue, pain, falls, abnormal coordination, numbness or tingling, sedation, sleepiness, tremor, confusion, disorientation, dissociation, abnormal speech, muscle spasms, nausea, vomiting, diarrhea, altered mood, depression, euphoric mood, hallucinations, blurred vision, dizziness, imbalance, palpitations, hypotension, syncope, urinary tract infection, allergic reactions, shortness of breath, lung infection, fever, sweatiness, headache
Time frame: 48 hours
Systolic and diastolic blood pressure in mmHg
Time frame: 48 hours
Heart rate in beats per minute
McMaster University
Other
The Pharmacokinetics of Oral Tetrahydrocannabinol and Cannabidiol Across the Spectrum of Glomerular Filtration Rate: a PharmacoKinetic Study
Acronym: POT-GFR-PK
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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