ACTRN12609001071213尚未招募4 期
A Case Series Investigating change in self-rated pain following Rotation to Methadone in Palliative Patients with Cancer Related Pain
Brisbane South Palliative Care Collaborative0 个研究点目标入组 20 人开始时间: 2009年12月14日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
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
- Non-randomised 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
- •*Patients reporting uncontrolled pain (defined as 4 or greater on a numerical rating scale 0-10 despite the use of regular background narcotics +/- adjuvants
- •*A component of the patients pain must be neoropathic as assessed using a validated neuropathic pain diagnostic assessment tool, the Douleur Neuropathique en 4 (DN4)
- •*Able to give informed consent in English
- •*Willing to be admitted to an inpatient facility for rotation to methadone
- •*Mini mental state exam (MMSE) score = or above 25/30
- •*Unsuitable for, or refusing, non-pharmacological interventions e.g. nerve blocks for pain
排除标准
- •*Patients less than 18 years of age
- •*Patients in whom the use of methadone is contraindicated e.g. using Monoamine oxidase inhibitors (MAOs), active alcoholism
- •*Patients with known risk factors for a prolonged QT interval
- •*Patients who have received treatments in the past 2 weeks likely to impact on pain levels e.g. chemotherapy, or who receive such therapy during the study period
- •*Changes in concomitant analgesic medication during the study period
- •*Any patient, in the opinion of the researchers, who is unable to comply with the study protocol
- •*Life expectancy less than 3 weeks
研究者
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