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临床试验/IRCT20180922041083N1
IRCT20180922041083N1已完成2 期

Comparison of the combined effect of Isosorbide with Misoprostol and Misoprostol alone on the cervical ripening in post-term pregnancy

Babol University of Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
150

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
18 years 至 40 years(—)
性别
Female

入选标准

  • Pregnant mothers from 18 to 40 years old
  • Bishop Score 6 and less with a range score of 0 to 13
  • Body mass in the first trimester of pregnancy in the normal range (26 - 19.8 kg . m2)
  • 41 weeks pregnancy based on ultrasonography of the first trimester of pregnancy
  • Singleton and cephalic pregnancy
  • Having a normal fetal heart rate or proper biophysical in 48 hours before entering the study

排除标准

  • Pregnant women with a history of headache
  • Misoprostol contraindications
  • Alcohol consumption
  • Preeclampsia and eclampsia
  • Uncontrolled diabetes
  • Intrauterine growth restriction
  • Polyhydramnios and oligohydramnios
  • Placenta previa or any other factor that prevents the induction of labor
  • Interaction medicine with Isosorbide

研究者

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