Actively Recruiting

Phase 2
Phase 3
Age: 19Years +
All Genders
NCT05786599

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

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

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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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Methadone to Treat Painful Chemotherapy Induced Peripheral Neuropathy | DecenTrialz