Actively Recruiting
Methadone to Treat Painful Chemotherapy Induced Peripheral Neuropathy
Led by University of British Columbia · Updated on 2025-03-27
50
Participants Needed
4
Research Sites
49 weeks
Total Duration
On this page
Sponsors
U
University of British Columbia
Lead Sponsor
B
British Columbia Cancer Agency
Collaborating Sponsor
AI-Summary
What this Trial Is About
Chemotherapy induced peripheral neuropathy (CIPN) or nerve pain, is a painful and debilitating complication which can chronically affect up to 70% of patients who receive chemotherapy. It causes "glove-and-stocking" distribution of nerve-pain, weakness, and other debilitating symptoms. This can affect patient's quality of life, function, ability to tolerate chemotherapy, and return to work. Duloxetine is the only recommended medication to reduce the painful symptoms and consequences of CIPN by national and international groups such as the American Society of Clinical Oncology. However, studies indicate it only has modest effect; for example, the largest study shows it only reduces pain by 0.73/10 points compared to placebo. Another promising medication in theory and practice is methadone. It is a commonly used and well-studied opioid with unique attributes which allows it to treat non-cancer and cancer associated nerve-pain with better efficacy when compared to other opioids. Furthermore, patients appear to develop less tolerance to methadone over time when compared to other opioids; this is helpful as many develop long-term CIPN and may greatly benefit from long-term pain medication. Therefore, if a patient requires chronic opioids to reduce the painful symptoms of CIPN, one that develops less tolerance is invaluable. Despite the promising role for methadone to treat CIPN, it has not been studied to treat this condition. Therefore, methadone may never be considered by prescribers to reduce the painful symptoms of CIPN. This study is a randomized controlled trial to assess the efficacy of methadone compared to duloxetine to treat painful CIPN. Participants will be randomized to receive either methadone or duloxetine regularly for 5 weeks. Methadone and duloxetine will be placed in indistinguishable capsules, so the participant and assessor are not aware of their treatment. They will be followed virtually or in-person weekly for 5 weeks where they will answer brief questionnaires detailing the effect of their treatment on their pain and their dose will increase weekly as tolerated until their pain is controlled or its the end of the study. This study would be critical in assessing the efficacy of a very promising medication to reduce the painful symptoms of CIPN: a debilitating disorder with otherwise few treatment options.
CONDITIONS
Official Title
Methadone to Treat Painful Chemotherapy Induced Peripheral Neuropathy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years old
- Estimated life expectancy greater than 12 weeks
- Opioid naive or oral morphine equivalent use less than 60 mg/day
- Greater than grade 1 CIPN based on CTCAE
- Average CIPN-related neuropathic pain greater than 3/10 lasting 3 months or more beyond chemotherapy completion
- Diagnosis of cancer
- Treatment with neurotoxic chemotherapies including platinums, taxanes, vinca alkaloids, bortezomib, or thalidomide
You will not qualify if you...
- Other causes of peripheral neuropathy
- Severe psychiatric illnesses including severe depression, suicidality, bipolar disorder, psychotic disorder, alcohol or substance use disorder, and eating disorders
- Medical illnesses such as mechanical gastrointestinal obstruction, surgical abdomen, acute or severe asthma, COPD, respiratory depression, delirium tremens, convulsive disorders, severe CNS depression, diarrhea from pseudomembranous colitis, and leptomeningeal disease
- Liver or renal dysfunction within the last 90 days as defined by MELD-Na score 17 or higher and GFR 30 ml/min or less
- QTc interval greater than 499 ms within the last 90 days
- Current pregnancy or lactation
- Inability to take oral medications
- Positive CAGE or Opioid Risk Tool - Revised questionnaire
- Known allergy or hypersensitivity to opioids, duloxetine, or any ingredient in their formulations
- Use of excluded medications such as methadone, other antidepressants, thioridazine, or potent CYP1A2 inhibitors
- Uncontrolled narrow-angle glaucoma
- Women of child-bearing potential unable or unwilling to use Health Canada approved highly effective contraception methods or abstinence during treatment period
AI-Screening
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Trial Site Locations
Total: 4 locations
1
Nanaimo Regional Hospital
Nanaimo, British Columbia, Canada
Not Yet Recruiting
2
BC Cancer Surrey
Surrey, British Columbia, Canada
Actively Recruiting
3
BC Cancer Vancouver
Vancouver, British Columbia, Canada, V5Z 4E6
Not Yet Recruiting
4
BC Cancer Victoria
Victoria, British Columbia, Canada
Not Yet Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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