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临床试验/CTRI/2021/09/036652
CTRI/2021/09/036652已完成未知

Sequential use of oral and vaginal misoprostol versus oral or vaginal misoprostol alone for Induction of labor and the caesarean delivery risk – A retrospective study

Dept Of Obstetrics And Gynecology0 个研究点目标入组 768 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
768

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Singleton with Cephalic presentation
  • Nulliparous and multiparous women who had completed 36 weeks of gestation
  • Modified Bishop’s score < 4
  • Normal fetal heart tracing available prior to induction

排除标准

  • 1. Documented Cephalopelvic disproportion
  • 2. Prior caesarean delivery/ previous scarring on the uterus
  • 3. Signs of labour (regular painful contractions with cervical change)
  • 4. Fetal demise or known major fetal anomaly
  • 5. Antepartum haemorrhage
  • 6. Cerclage in the current pregnancy
  • 7. Oligohydramnios, defined as amniotic fluid index < 5 cm or maximal vertical pocket < 2 cm
  • 8. Fetal growth restriction, defined as EFW < 10th percentile
  • 9. Chronic medical disorders i.e., chronic hypertension, pregestational diabetes mellitus, renal diseases

研究者

发起方
Dept Of Obstetrics And Gynecology

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