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临床试验/ISRCTN33846889
ISRCTN33846889已完成不适用

Randomised prospective study comparing epidural analgesia perioperatively and 24 hours preoperatively for the prevention of postoperative stump pain and phantom limb pain following major amputation

Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)0 个研究点目标入组 40 人开始时间: 2004年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Patients above the age of 18
  • 2. All patients undergoing scheduled lower limb amputation will be considered

排除标准

  • 1. Non general anaesthetic (GA)
  • 2. Emergency surgery
  • 3. Unable to give consent
  • 4. Contraindications to epidural
  • 5. Anticoagulated

研究者

发起方
Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)

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