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临床试验/ACTRN12606000073505
ACTRN12606000073505尚未招募4 期

A randomised, open-label, single centre, cross-over study to assess the efficacy and safety of methoxyflurane for the treatment of incident pain in patients undergoing radiotherapy

Peter MacCallum Cancer Centre0 个研究点目标入组 50 人开始时间: 2006年2月22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
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 75 Years(—)
性别
Female

入选标准

  • Radiotherapy related incident/movement pain; age: ECOG <=2.

排除标准

  • Renal imparirment (>2xnormal); previous toxicity or use of methoxyflurane; family or personal history of hyperthermia or sensitivites to flourinated anaesthetics; patients receiving Patient Controlled Analgesia.

研究者

发起方
Peter MacCallum Cancer Centre

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