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临床试验/IRCT20201024049128N1
IRCT20201024049128N1招募中4 期

A Comparative Study about Maternal and Neonatal Outcomes of Using Extra-Amniotic Saline Infusion and vaginal Misoprostol for Cervical Ripening and Labor Induction in Pregnant Women with Unfavorable Cervix

Karaj University of Medical Sciences0 个研究点目标入组 144 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
144

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

年龄范围
no limit 至 no limit(—)
性别
Female

入选标准

  • Singleton gestation
  • Alive fetus
  • Cephalic presentation
  • Intact membranes
  • Unfavorable cervix (Bishopscore =6)
  • Reassuring fetal heart rate
  • Gestational age=28

排除标准

  • Non-cephalic presentation
  • Adequate uterine contractions (3 contractions Lasting for 30sec/10 min)
  • Ruptured membranes
  • Cephalopelvic disproportion
  • Multiple pregnancy
  • Polyhydramnios
  • Estimated fetal weight =4000g or =1800g
  • Placental abruption, Placenta previa
  • Unexplained vaginal bleeding
  • Prior lower segment cesarean section/Scarred uterus
  • Non-reassuring fetal status
  • Clinically detected vaginal infections(exp:genital herpes) or chorioamnionitis
  • Latex or Prostaglandins allergy or any contraindications receiving Prostaglandins, including a history of asthma, glaucoma, or cardiovascular disease
  • Intrauterine fetal death
  • Renal or hepatic failure

研究者

发起方
Karaj University of Medical Sciences

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