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临床试验/EUCTR2015-002942-30-DK
EUCTR2015-002942-30-DK进行中(未招募)1 期

CONDISOX: Continued versus discontinued oxytocin stimulation of labour in a double-blind randomised controlled trial

Regional Hospital of Randers0 个研究点目标入组 1,700 人开始时间: 2015年10月14日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
1,700

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

  • Women stimulated with Syntocinon® infusion for induction of labour (with or without cervical priming by prostaglandin and a cervical dilatation of = 4cm).
  • 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 1200
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Unable to read and understand the Danish language or to give informed consent
  • Non-cephalic presentation
  • Multiple gestation
  • Pathological fetal heart rate pattern (cardiotocogram, CTG) before Syntocinon® initiation
  • Fetal weight estimation > 4500 g (clinical or ultrasonic)
  • Subject declines participation
  • Gestational age less than 37 completed weeks

研究者

发起方
Regional Hospital of Randers

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