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临床试验/ACTRN12615001299594
ACTRN12615001299594招募中4 期

The effect of timing of intramuscular oxytocin administration on neonatal arterial oxygen saturation during delayed cord clamping in vaginal births. at term

Monash Health0 个研究点目标入组 192 人开始时间: 2015年11月30日最近更新:

试验速览

阶段
4 期
状态
招募中
发起方
Monash Health
入组人数
192

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention

入排标准

年龄范围
18 Years 至 50 Years(—)
性别
Female

入选标准

  • To be eligible to participate in the trial, women must:
  • 1) Over the age of 18
  • 2) Under the age of 50
  • 3) 37 weeks pregnant or more
  • 4) Singleton pregnancy
  • 5) Vaginal birth at term
  • 6) Be capable of understanding the information provided
  • 7) Give written informed consent

排除标准

  • Women who meet any of the following criteria at any point during the trial will not be eligible to participate:
  • 1) Multiple gestation
  • 2) Previous post partum haemorrhage (blood loss of >500 mL following vaginal birth or > 750 mL following caesarean section)
  • 3) Detected congenital disorders or intrauterine growth restriction
  • 4) Possession of contraindicating factors for the use of oxytocin
  • 5) Possession of significant risk factors for post partum haemorrhage (e.g. macrosomia >4.5kg, polyhydramnios, abnormal placentation, emergency caesarean section)

研究者

发起方
Monash Health

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