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临床试验/NCT01686347
NCT01686347终止4 期

Epidural Analgesia and Troubles of Fetal Cardiaq Rythm : Effect of the Systemic Transfer of Ropivacaine and Sufentanil

University Hospital, Rouen2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2012年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
发起方
入组人数
40
试验地点
2
主要终点
Plasmatic concentrations compared maternal ropivacaine based on the presence of abnormal fetal heart rate

研究概览

简要总结

The aim of the investigators study is to demonstrate the association between fetal cardiac rhythm abnormalies after epidural analgesia and the maternal systemic transfer of ropivacaine and/or sufentanil.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 18 years old or more
  • nulliparous
  • _ one fetus
  • head first
  • spontaneous labor
  • epidural analgesia
  • no fetal cardiac rhythm abnormalies before the epidural analgesia
  • no active management of labor during 30 minutes after the epidural analgesia induction
  • signature of the consent form

排除标准

  • pathological pregnancy
  • low maternal blood pressure during the 30 minutes after the epidural analgesia
  • uterin contraction which last for 5 minutes or more
  • more than 6 uterin contractions during a 10 minutes period
  • Ropivacaine contraindication
  • sufentanil contraindication

研究组 & 干预措施

control group

Other

patient at term, spontaneous labor, without any fetal cardiac rhythm abnormalies during the 30 minutes after the epidural analgesia induction

干预措施: ropivacaine (Drug)

fetal cardiac rhythm abnormally

Other

patient at term, in spontanous labor with fetal cardiac rythm abnormally which occurs 30 minutes after the epidural analgesia induction

干预措施: ropivacaine (Drug)

结局指标

主要结局

Plasmatic concentrations compared maternal ropivacaine based on the presence of abnormal fetal heart rate

时间窗: 1 day

Maternal Plasmatic concentrations of ropivacaine will be measured in mg / liter of maternal blood and the median of each group will be compared by paired Wilcoxon test

次要结局

  • Plasmatic concentrations compared maternal sufentanil based on the presence of abnormal fetal heart rate(1 day)

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (2)

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