跳至主要内容
临床试验/EUCTR2005-004577-23-NO
EUCTR2005-004577-23-NO进行中(未招募)不适用

Remifentanil as pain relief during labour

niversitetet i Bergen0 个研究点开始时间: 2005年10月31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

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

  • Healthy primiparaous woman with a normal pregnancy coming to full term labour, wishing pain relief to stand the labour pain.
  • 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

  • Abnormal pregnancy or labour (Hypertension, bleeding disturbances, pregnancy intoxication, multiple foetous, abnormal foetus)
  • Any other opioid given within the 8 last hours before study start

研究者

发起方
niversitetet i Bergen

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