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临床试验/IRCT2012080610511N1
IRCT2012080610511N1已完成2 期

Comparison of characteristics of women undergoing labor induction with oxytocin and oral misoprostol

Shahid Beheshti University of Medical Sciences0 个研究点目标入组 65 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
65

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
17 years 至 36 years(—)
性别
Female

入选标准

  • 39 to 42 weeks of gestational age; Estimated fetal weight 4000 g; Normal fetal heart rate; cephalic presentation; Absence of uterine contractions; Singleton pregnancy; Bishop score of 7 or less. Exclusion criteria: Previous uterine surgery including caesarean section; Intrauterine fetal death IUGR; Oligohidroamnius; Placenta previa; Umbilical cord Prolapse; Corioamnionitis symptoms; Symptoms of active herpes; kidney or liver disease; NST Non-Stress Test reactive bread; Contraindication for Administration of prostaglandin. Contraindication for induction of labor; Vaginal bleeding of unknown cause.

排除标准

  • 未提供

研究者

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