ACTRN12616000739415终止未知
Comparison of low-risk pregnant women undergoing induction of labour at term by outpatient balloon or inpatient prostaglandin in order to assess caesarean section rate; a randomised controlled trial
Department of Obstetrics and Gynaecology, FMHS, University of Auckland0 个研究点目标入组 1,087 人开始时间: 2016年6月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 终止
- 发起方
- 入组人数
- 1,087
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
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 16 Years 至 50 Years（—）
- 性别
- Female
入选标准
- •Women with a live singleton cephalic presentation planning induction of labour at 37 weeks’ gestation or more
排除标准
- •major congenital anomaly; suspected severe fetal growth restriction (defined as estimated fetal weight less than 10th centile or abdominal circumference less than or equal to 5th centile AND oligohydramnios or abnormal dopplers, OR estimated fetal weight less than 3rd centile); previous caesarean; ruptured membranes; bishop score 7 or more at commencement of induction; maternal risk or fetal compromise that would necessitate monitoring the woman or her baby in hospital; not willing to stay within 60 minutes of hospital; does not speak English or have someone with them who speaks English.
研究者
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