Cannabidiol for Pain Relief of Patients With End-stage mCRPC
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Cannabidiol, Placebo.
- Who it may be relevant to
- Registry conditions: Metastatic Castration Resistant Prostate Cancer (mCRPC). Basic parameters: No limits · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Denmark
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Efficacy and Safety of Cannabidiol for Pain Relief of Patients With End-stage Metastatic Castration Resistant Prostate Cancer - a Randomised Double-blinded Placebo-controlled Phase II Trial
Overview
The goal of this clinical trial is to evaluate the effects of cannabidiol in patients with end-stage metastatic castration-resistant prostate cancer (mCRPC). The primary objective is to determine whether cannabidiol (CBD) treatment can reduce the need for opioids in patients with end-stage mCRPC. Additionally, the study will assess a range of clinical endpoints in patients with end-stage mCRPC, including: 1. The efficacy of CBD treatment in alleviating pain 2. The efficacy of CBD treatment in reducing the need for non-opioid medications and concomitant therapies 3. The impact of CBD treatment on physical activity and quality of life 4. The anti-inflammatory and potential anti-tumor properties of CBD 5. The safety of CBD treatment Patients from Department of Urology, Aalborg University Hospital will be included. Participants will be treated with either CBD (200 mg) or placebo (0 mg) three times daily for nine weeks. At baseline, halfway and end of trial, participants will use an activity tracker and complete questionnaires regarding pain and quality of life and provide blood samples to measure inflammation and tumor activity. Also, they will complete a daily dairy regarding the study drug and intake of pain medication. Adverse events will be assessed by Common Terminology Criteria for Adverse Events.
Interventions
- Drug Cannabidiol
Name: Cannabidiol, 100 mg/ml Dosage: 2 ml three times a day (=600 mg CBD/day) Administration form: oil (oral) - Drug Placebo
Name: Placebo Dosage: 2 ml three times a day (=0 mg CBD/day) Administration form: oil (oral)
Primary outcome measures
- Total daily dose of opioids (morphine milligram equivalents) [Time frame: Baseline and 9 weeks]
Secondary outcome measures (10)
- Worst pain intensity on numeric rating scale (NRS) [Time frame: Baseline and 9 weeks]
- Interference of pain on daily functioning [Time frame: Baseline and 9 weeks]
- Total daily dose of non-opioid analgesics [Time frame: Baseline and 9 weeks]
- Use of concomitant therapy [Time frame: Baseline and 9 weeks]
- Quality of life by EORTC-QLQ-C30 [Time frame: Baseline and 9 weeks]
- Quality of life by EORTC-QLQ-PR25 [Time frame: Baseline and 9 weeks]
- Physical activity [Time frame: Baseline and 9 weeks]
- Tumour activity [Time frame: Baseline and 9 weeks]
- Inflammation [Time frame: Baseline and 9 weeks]
- Safety profile outcomes [Time frame: Baseline and 9 weeks]
Eligibility criteria
Inclusion criteria
- Patients diagnosed with mCRPC as documented by increasing PSA despite optimally attempted treatment, and no other therapeutic options.
- Treatment-resistance or ineligible to standardized cancer therapy, incl. medical and surgical castration, chemotherapy, and super hormone treatment.
- Minimum 3 months since radiation therapy, if part of treatment.
- Perception of pain
- Daily use of Morphine (ATC: N02AA01) (10mgx2) in relief of pain.
Exclusion criteria
- Perception of worst pain <4.0 on the NRS within the last week prior to baseline visit70. (Inclusion if: three days with highest pain intensity have an average of ≥4.0 and/or three days where pain intensity is at least 4.0).
- Pattern of short duration of response to all previous treatment regimens (<6 months) clinically assessed by the investigator.
- Eastern Cooperative Oncology Group (ECOG) performance status >3 (scale 0-5).
- Change in regular use of conventional pain medication within two weeks prior to baseline visit.
- A history of substance use disorder.
- Functional liver insufficiency with an alanine transaminase (ALT) >2X ULN and/or bilirubin >2X ULN assessed by a blood sample taken at screening.
- Renal failure with an estimated glomerular filtration rate (eGFR) < 30mL/min/1,73m2 assessed by a blood sample taken at screening.
- Known heart failure - New York Heart Association III - IV (scale I-IV)71.
- Known severe chronic obstructive lung disease (Forced Expiratory Volume in the first second (FEV1) <50%)72.
- Use of THC-containing cannabis products measured by a urine sample at screening.
- Any chronic or acute systemic medical condition that, in the opinion of the investigator, may pose a risk to the safety of the patient or may interfere with compliance or the assessment of efficacy in this trial.
- Hypersensitivity to the active substance
- Not capable of giving informed consent.
- Not capable of understanding, write or read Danish.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Quadruple blind
- Primary purpose
- Supportive care
Study locations
Denmark · 1 center
- Department of Urology, Aalborg University Hospital — Gistrup
Identifiers
NCT: NCT07549256 · 2024-513951-33-00 · 2024-513951-33-00 · F2024-111