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临床试验/ACTRN12609001071213
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

发起方
Brisbane South Palliative Care Collaborative

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