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临床试验/ACTRN12618000510246
ACTRN12618000510246尚未招募未知

Amongst women undergoing induction of labour using a balloon catheter, is leaving the balloon in for 6 hours, compared to 12 hours, associated with similar changes in the cervix to prepare for labour, similar clinical outcomes, and a similar healthcare experience?

Mater Misericordiae Ltd0 个研究点目标入组 858 人开始时间: 2018年4月9日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
858

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
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Female

入选标准

  • All women with live singleton pregnancies greater than or equal to 37+0 weeks booked for induction of labour and requiring cervical priming (i.e. the cervix to be softer, shorter, dilated)

排除标准

  • Major congenital abnormality; multiple pregnancy; fetal death in utero; any contraindication to vaginal birth; previous caesarean section; modified Bishops score of 7 or more at commencement of induction of labour; women <18 years; inability to consent.

研究者

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