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临床试验/ISRCTN97113005
ISRCTN97113005已完成未知

Induction of labour at 39 weeks or beyond in nulliparous women with a sonographically favourable cervix: a randomised control trial

niversity of Malaya0 个研究点目标入组 179 人开始时间: 2021年10月6日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
179

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. Aged 18 years and above
  • 2. Gestational age of 38 weeks to 39 weeks 6 days at enrolment
  • 3. No other intervention currently required or anticipated
  • 4. No medical contraindication to induction of labour.
  • 5. Sonographically favourable cervix (cervical length less than 27 mm by vaginal scan)
  • 6. Nulliparous
  • 7. Singleton with live fetus
  • 8. Cephalic presentation
  • 9. Written informed consent
  • 10. Willingness to participate in the trial

排除标准

  • 1. Women with a known lethal fetal congenital abnormality
  • 2. Previous uterine surgery or uterine injury
  • 3. Indication for early or urgent delivery
  • 4. Contraindication for vaginal delivery
  • 5. Medical complications during pregnancy
  • 6. Women who book late for antenatal care and have no dating scan performed before 22 weeks to provide an accurate expected delivery date

研究者

发起方
niversity of Malaya

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