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临床试验/CTRI/2021/03/032211
CTRI/2021/03/032211尚未招募3 期

Role of Mifepristone in cervical ripening for induction of labour in non high risk pregnant women - A Double Blind Randomized Controlled Trial

SHAILY TYAGI0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方

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

入选标准

  • Patients giving consent for study
  • Singleton pregnancy
  • Gestational age >= 40 completed weeks (Gestation age confirmed by earliest ultrasound and reliable date of last menstrual period) with cephalic presentation
  • Adequate pelvis
  • Bishop score <6
  • Reactive NST
  • Age >18 â?? 35 year.

排除标准

  • Patients not giving consent for the study
  • Multiple pregnancy
  • Any obstetrics contraindication for induction of labour (previous scar on uterus, any coagulation failure, placenta previa)
  • Patients with any other associated medical condition like gestational diabetes mellitus, hypertension, sepsis, pyrexia, disease which contraindicates the use of mifepristone like adrenal insufficiency
  • Estimated fetal weight >= 4kg
  • Oligohydromnios
  • Fetal growth restriction.

研究者

发起方
SHAILY TYAGI

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