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Active, Not Recruiting

NCT Number: NCT05742724

The Pharmacokinetics of Single Dose Oral Tetrahydrocannabinol and Cannabidiol

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • adult age>25 years
  • estimated glomerular filtration rate (eGFR)>60ml/min/1.73m2 or eGFR<60ml/min/1.73m2 by the CKD Epidemiology Collaboration equation including in-center hemodialysis at least 2x weekly for a minimum of 3 hours per treatment via a tunnelled catheter treated >90 days
  • agree to take the medication as directed in the study
  • provides informed consent

Exclusion criteria

  • body mass index <20 or >35kg/m2
  • physical dependence on any drug other than caffeine or nicotine
  • history of clinically significant adverse event associated with cannabis intoxication
  • history of psychosis or mania or any active major psychiatric disorder
  • recent (within 30 days) use of any cannabinoid (natural or synthetic) identified by self-report or urine drug screen for cannabinoids
  • taking any medication with known interactions with THC or CBD via cytochrome P450 (CYP) CYP2C9, CYP2C19 and CYP4A6 or CYP2D4 (e.g. anti-epileptic drugs, calcineurin inhibitors, anti-fungal)
  • evidence of liver dysfunction (ALT less than 3 times upper limit of normal, bilirubin below upper limit of normal, international normalized ratio<1.5)
  • pregnant or breastfeeding women
  • change in ideal body weight or dry weight in the last 4 weeks
  • intradialytic hypotension (systolic blood pressure<90mmHg) requiring an intervention in the previous 4 weeks

Treatment and study plan

Tetrahydrocannabinol-Cannabidiol Combination

Drug

Oral THC 0.1mg/kg and CBD 2.5mg/kg

Primary outcomes

  1. Tetrahydrocannabinol and its metabolites maximum concentration (Cmax)

    Time frame: 48 hours

    Maximum concentration (Cmax)

  2. Tetrahydrocannabinol and its metabolites time to Cmax

    Time frame: 48 hours

    Time to Cmax

  3. Tetrahydrocannabinol and its metabolites last detection time

    Time frame: 48 hours

    Last detection time

  4. Tetrahydrocannabinol and its metabolites area under the curve

    Time frame: 48 hours

    Area under the curve

  5. Tetrahydrocannabinol and its metabolites renal clearance

    Time frame: 48 hours

    Renal clearance

  6. Tetrahydrocannabinol and its metabolites dialytic clearance

    Time frame: 48 hours

    Dialytic clearance

  7. Cannabidiol and its metabolites maximum concentration (Cmax)

    Time frame: 48 hours

    Maximum concentration (Cmax)

  8. Cannabidiol and its metabolites time to Cmax

    Time frame: 48 hours

    Time to Cmax

  9. Cannabidiol and its metabolites last detection time

    Time frame: 48 hours

    Last detection time

  10. Cannabidiol and its metabolites area under the curve

    Time frame: 48 hours

    Area under the curve

  11. Cannabidiol and its metabolites renal clearance

    Time frame: 48 hours

    Renal clearance

  12. Cannabidiol and its metabolites dialytic clearance

    Time frame: 48 hours

    Dialytic clearance

  13. Other cannabinoids and their metabolites maximum concentration (Cmax)

    Time frame: 48 hours

    Maximum concentration (Cmax)

  14. Other cannabinoids and their metabolites time to Cmax

    Time frame: 48 hours

    Time to Cmax

  15. Other cannabinoids and their metabolites last detection time

    Time frame: 48 hours

    Last detection time

  16. Other cannabinoids and their metabolites area under the curve

    Time frame: 48 hours

    Area under the curve

  17. Other cannabinoids and their metabolites renal clearance

    Time frame: 48 hours

    Renal clearance

  18. Other cannabinoids and their metabolites dialytic clearance

    Time frame: 48 hours

    Dialytic clearance

Secondary outcomes

  1. Adverse events

    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

  2. Blood pressure

    Time frame: 48 hours

    Systolic and diastolic blood pressure in mmHg

  3. Heart rate

    Time frame: 48 hours

    Heart rate in beats per minute

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Collaborators

  • Center for Medicinal Cannabis Research

Registry information

Official study title

The Pharmacokinetics of Oral Tetrahydrocannabinol and Cannabidiol Across the Spectrum of Glomerular Filtration Rate: a PharmacoKinetic Study

Acronym: POT-GFR-PK

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Feb 24, 2023
Registry last updated
Nov 20, 2024

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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