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临床试验/EUCTR2011-004702-17-IE
EUCTR2011-004702-17-IE进行中(未招募)不适用

Comparison of Ultrasound - Guided Continuous Rectus Sheath Blockade and Continuous Preperitoneal Wound Catheter Infiltration of Local Anaesthetic for Postoperative Analgesia following Laparotomy.

Department of Anaesthesia0 个研究点开始时间: 2011年11月4日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)

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 general surgical patients presenting for laparotomy
  • Written informed consent
  • 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 60
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 60

排除标准

  • Patient refusal.
  • Local infection at site of insertion.
  • Allergy to amide local anaesthetics, opioids, paracetamol, NSAIDs, ketamine, NMBs, volatile anaesthetics.
  • Concurrent use of antiarrhythmics with local anaesthetic activity.
  • Concurrent use of MAOIs or within 2 weeks of MAOI use.
  • Severe liver or cardiac dysfunction.
  • Inability to comprehend pain scoring system.
  • Elderly or debilitated patients that require a reduction in levobupivacaine dose commensurate with their physical status, resulting in the protocol not being followed.

研究者

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