跳至主要内容
临床试验/EUCTR2006-004053-20-IE
EUCTR2006-004053-20-IE进行中(未招募)不适用

Determination of the efficacy of the Transversus Abdominis Plane (TAP) Block in the management of postoperative pain following Caesarean Section. - TAP post LSCS

Dept of Anaesthesia, University College Hospital, Galway0 个研究点开始时间: 2006年9月20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)
发起方

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
Female

入选标准

  • Adult Females aged >18 years old
  • Presenting for elective or emergent Caesarean Section
  • Written Informed Consent
  • ASA Grade 1 to 3
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patient refusal
  • Severe Pregnancy related diseases such as Pre-Eclamsia, HELLP.
  • Outside Age Range
  • Allergy to bupivacaine, morphine, paracetamol, diclofenac sodium
  • Skin lesions/infection at site of injection
  • Renal or other organ dysfunction

研究者

发起方
Dept of Anaesthesia, University College Hospital, Galway

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