跳至主要内容
临床试验/ACTRN12621000141842
ACTRN12621000141842尚未招募2 期

An Exploratory Randomised Controlled Open-Label Study of Methadone Rotation versus Other Opioid Rotation for the Treatment of Refractory Cancer Induced Bone Pain

Dr Merlina Sulistio0 个研究点目标入组 50 人开始时间: 2021年2月11日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Age at least 18 years.
  • Diagnosis of solid tumour or haematological cancer with a predicted prognosis of greater than 8 weeks.
  • Diagnosis of CIBP confirmed through radiological investigations and meeting the core diagnostic criteria for CIBP as defined by The Analgesic, Anesthetic, and Addiction Clinical Trial Translations, Innovations, Opportunities, and Networks-American Pain Society (ACTTION-APS).
  • On a strong baseline opioid pre-rotation (morphine, oxycodone or hydromorphone).
  • Willing to be enrolled in a trial comparing methadone to another opioid rotation, where allocation is at random (1:1).
  • greater than or equal to 4 of 10 worst pain from CIBP on 0 to 10 numeric rating scale (NRS) and/ or existing opioid results in opioid toxicity (CTCAE grade 2 or greater).
  • Sufficiently proficient in English to be able to complete questionnaires and provide informed consent.

排除标准

  • Received radiotherapy in the last 30 days.
  • QTc >500msec.
  • History of mental health condition or impaired cognition that would prevent completion of questionnaires.
  • Too unwell to participate in the study as determined by the patient’s treating physician.

研究者

发起方
Dr Merlina Sulistio

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