跳至主要内容
临床试验/EUCTR2008-006080-36-GB
EUCTR2008-006080-36-GB进行中(未招募)不适用

Analgesic efficacy of ultrasound guided transversus abdominis plane block as part of a multimodal analgesic regime for post elective caesarean section pain – a comparative double-blinded placebo controlled trial using plain bupivacaine, bupivacaine with adrenaline and bupivacaine with dexamethasone. - Do adjuncts in TAP blocks prolong analgesia post caesarean section?

Portsmouth Hospitals NHS Trust0 个研究点开始时间: 2009年1月19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
Female

入选标准

  • 1)women undergoing elective caesarean section at St Mary’s Hospital who are able to receive the standard anaesthetic and analgesic regime
  • 2)women who are fit and well or who have only mild to moderate functional disability ( ASA 1 or 2)
  • 3)women aged between 18 and 50 years of age
  • 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

  • 1)women unable to receive the standard regime ie severe pre-eclampsia, coagulopathy, local anaesthetic allergy, non-steroidal anti-inflammatory drug intolerance
  • 2)patients with an early pregnancy (booking) body mass index of >40
  • 3)patients who are immunocompromised
  • 4)patients weighing <50kg
  • 5)patients with diabetes requiring insulin
  • 6)patients taking any drugs with analgesic activity
  • 7)women at the extremes of reproductive age: less than 18 years and greater than 50 years

研究者

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