ISRCTN16222339进行中（未招募）未知
Randomised controlled trial of 4 hourly versus 8 hourly vaginal examination interval after amniotomy and cervical ripening with Foley's catheter in nulliparas
niversity Malaya Medical Centre0 个研究点目标入组 198 人开始时间: 2021年5月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 198
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Women who had cervical ripening with Foley catheter only and favourable cervix with cervical dilatation of 3cm or greater (suitable for amniotomy) with contraction <1:5min
- •2. Nulliparous
- •3. No prior pregnancy beyond 20 weeks gestation
- •4. Age 18 years and above
- •5. Gestational age of =37weeks at enrolment scheduled induction of labour
- •6. Scheduled induction of labour
- •7. Viable pregnancy
- •8. Cephalic presentation
- •9. Singleton pregnancy
- •10. Reassuring pre induction fetal cardiotocography (CTG)
- •11. Intact membrane
排除标准
- •1. Contraindication to vaginal delivery
- •2. Known gross fetal anomaly
- •3. Fetal weight clinically estimated to be =2 kg & =4kg and confirmed by ultrasound
- •4. Previous uterine surgery, ie: myomectomy, hysterotomy and history of iatrogenic uterine perforation
研究者
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