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临床试验/ISRCTN15309710
ISRCTN15309710进行中(未招募)未知

Randomised controlled trial of 4 hours versus 8 hours vaginal examination intervals after amniotomy and cervical ripening with Foleys catheter in multiparous women

niversity Malaya Medical Centre0 个研究点目标入组 202 人开始时间: 2021年10月7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
202

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. Multiparous women
  • 2. Aged 18 years and above
  • 3. Gestational age of =37 weeks at enrolment of scheduled induction of labour
  • 4. Cephalic presentation
  • 5. Singleton pregnancy
  • 6. Women who had cervical ripening with Foleys catheter and favourable cervix with cervical dilatation of 3 cm or greater (suitable for amniotomy) with contraction <1:10
  • 7. Reassuring fetal cardiotocography (CTG) tracing

排除标准

  • 1. Previous uterine incision/injury (caesarean delivery, myomectomy, perforation)
  • 2. Gross fetal anomaly
  • 3. Contraindication for vaginal birth
  • 4. Estimated fetal weight =4.0 kg before induction

研究者

发起方
niversity Malaya Medical Centre

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