ACTRN12615001173583尚未招募2 期
The effect of cessation of intravenous oxytocin in women who have had an induction of labour with intravenous oxytocin and a spontaneous vaginal delivery, on postpartum measured blood loss: a three armed randomised controlled trial
Curtin University School of Nursing Midwifery and Paramedicine0 个研究点目标入组 312 人开始时间: 2015年11月2日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 312
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
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 16 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Women would be included in the study if they:
- •Are more than or equal to 16 years old.
- •Receive intrapartum oxytocin for induction of labour.
- •Have a singleton pregnancy.
- •Are more than or equal to 37 weeks gestation.
- •Have a spontaneous vaginal delivery.
排除标准
- •Women would be excluded from the study if they:
- •Are <16 years old.
- •Have a multiple pregnancy.
- •Are <37 weeks gestation.
- •Commence intravenous oxytocin as part of the postpartum haemorrhage regime.
- •Have an assisted vaginal delivery.
- •Have a caesarean section.
- •Have their intravenous oxytocin ceased before delivery.
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