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临床试验/EUCTR2010-020020-21-GB
EUCTR2010-020020-21-GB
进行中(未招募)
1 期

Comparison of the ED95 dose of 0.075% and 0.1% bupivacaine for labour analgesia in primigravida - MED and Epidural Bupivacaine

eeds Teaching Hospitals Trust0 个研究点目标入组 100 人开始时间: 2011年4月15日最近更新:

概览

阶段
1 期
状态
进行中(未招募)
发起方
eeds Teaching Hospitals Trust
入组人数
100

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

入选标准

  • ASA 1\-3 patients
  • Age \> 18 years
  • Primigravida (1st pregnancy) patients requesting epidural analgesia in early labour (\= 5 cm cervical dilatation
  • 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

  • Primigravida (1st pregnancy) patients requesting epidural analgesia in late labour (\> 5 cm cervical dilatation)
  • Multigravida patients ( \= 2nd pregnancy)
  • Age \< 18 years
  • Allergy to Bupivacaine
  • Unable to give written informed consent
  • Abnormal blood coagulation profile
  • Patients taking any medication that are indicated in the SPC as not recommended

研究者

发起方
eeds Teaching Hospitals Trust

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