跳至主要内容
临床试验/EUCTR2006-005802-29-GB
EUCTR2006-005802-29-GB进行中(未招募)不适用

Postoperative analgesia for Total knee replacement: A comparision between intrathecal morphine and peripheral nerve block.

Gwent Healthcare NHS Trust0 个研究点目标入组 80 人开始时间: 2011年6月27日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Adult patients of ASA physical status I to III undergoing elective primary unilateral Total Knee Replacement surgery.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • The exclusion criteria include patients who refuse consent, revision surgery,history of adverse reaction or a contraindication to the administration of morphine, local anaesthetics,non steriodal anti-inflammatory drugs,paracetamol, tramadol, centrineuraxial block and peripheral nerve blocks.Pateints with history of chronic pain other than at the site of joint replacement and on strong regular opiods.Renal impairment , liver impairment, ASA physical status greater than III and weight below 60 kgs.

研究者

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