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临床试验/NL-OMON51769
NL-OMON51769撤回3 期

Mild induced labour prior to planned caesarean delivery to improve neonatal outcome - a randomized trial (Lacarus) - Lacarus

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
撤回
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 0(—)

入选标准

  • * singleton pregnancy
  • * ECS without preceding contractions or rupture of the membranes
  • * Absence of a contraindication to oxytocin.
  • * Informed Consent as documented by signature.

排除标准

  • Non-inclusion criteria mother:
  • * Known or suspected unwillingness to follow the protocol
  • * Substance abuse (for example heroin, cocaine, amphetamine)
  • * Placenta praevia
  • * Clinical signs of infection
  • * Treated hypertension
  • * Preeclampsia
  • * Diabetes type I or II
  • * Steroid therapy during pregnancy
  • * Betablocker intake at inclusion
  • * Antenatal steroid administration for lung maturation
  • * A history of more than one previous caesarean section
  • Non-inclusion criteria fetus:
  • * Chromosomal aberration
  • * Malformation
  • * Nonreassuring fetal heart rate pattern

研究者

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