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?
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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