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Methadone to Treat Painful Chemotherapy Induced Peripheral Neuropathy

Study acronym: METACIN
StatusRecruiting
PhasePhase 2/3
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated March 27, 2025 (before its estimated March 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Notable Trial status: Not Yet Recruiting to Recruitingv5 Show 4 more changesShow less
    • Start date changed from estimate of May 2024 to Mar 21, 2025
    • Primary and study completion dates: Feb 2026 to Mar 2026
    • Eligibility criteria expanded, about 170 words
    • Study description expanded, about 12 words
  2. Notable Phase: Phase 2 to Phase 2/3v4 Show 11 more changesShow less
    • Enrollment target: 20 to 50
    • Primary completion date: Jun 2025 to Feb 2026
    • Primary endpoint revised
    • Study completion date: Aug 2025 to Feb 2026
    • Start date: Jul 2024 to May 2024
    • Interventions: Methadone (Drug) to duloxetine (Drug), methadone (Drug)
    • Secondary endpoints revised (2)
    • Study description expanded, about 333 words
    • Study arms: 1 to 2
    • Eligibility criteria expanded, about 3 words
    • Study title expanded, about 1 word
  3. Notable Primary completion date: Jun 2024 to Jun 2025
    • Start date: Jul 2023 to Jul 2024
    • Study completion date: Aug 2024 to Aug 2025
    v3
  4. Minor Re-verified, no change to tracked fieldsv2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05786599
Lead Sponsor University of British Columbia
Collaborators: British Columbia Cancer Agency
Conditions
(from sponsor)
Chemotherapy-induced Peripheral Neuropathy
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov