ACTRN12614000039684终止未知
Amongst women with singleton uncomplicated pregnancies greater than or equal to 37 weeks 0 days undergoing induction of labour (IOL) for post-term pregnancy or for ‘social’ or ‘elective’ reasons, does the use of a balloon-catheter to commence an IOL as an outpatient, compared with prostaglandin vaginal gel administration to commence an IOL as an inpatient, improve perinatal health outcomes, reduce length of stay and other healthcare costs, and is it preferred by women?
Mater Research0 个研究点目标入组 695 人开始时间: 2014年1月16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
- 695
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 52 Years（—）
- 性别
- Female
入选标准
- •All women with live singleton pregnancies greater than or equal to 37 weeks 0 days, booked for induction of labour because of post-term and/or social/elective reasons, and requiring cervical priming will be suitable for inclusion in this study
排除标准
- •Major congenital abnormality
- •Multiple pregnancy
- •Intrauterine fetal death
- •Clinical suspicion or ultrasound diagnosis of fetal growth restriction
- •Any contraindication to vaginal birth
- •Indication for IOL other than post-term and/or social/elective reasons
- •Modified Bishops score = 7 at commencement of IOL
- •Women <18 years
- •Inability to consent
研究者
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