跳至主要内容
临床试验/EUCTR2006-001033-18-GB
EUCTR2006-001033-18-GB进行中(未招募)不适用

Extending low-dose epidural for emergency Caesarean section - a comparison of bicarbonated lidocaine with 0.5% levobupivacaine

Chelsea and Westminster Hospital0 个研究点目标入组 100 人开始时间: 2006年4月10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
入组人数
100

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

  • Inclusion criteria will be established labour beyond 36 weeks gestation and women requesting an epidural for pain relief in labour.
  • 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

  • Exclusion critera will be an epidural top-up of solution stronger than bupivacaine 0.1% within the previous hour, pehtidine in the last 4 hours, multiple preganct, pre-eclampsia, antepartum haemmorage, cardiac disease, any contra-indication to regional analgesia or anaesthesia and any allergy to non-steroidal anti-inflammatory drugs

研究者

发起方
Chelsea and Westminster Hospital

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