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
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