IRCT2015122425648N2已完成未知
The efficacy of misoprostol and oxytocin for induction of labor
Vice Chancellor for Research of Mashhad University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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
- •Inclusion criteria are: mothers desire to have vaginal delivery, gestational age of 41 weeks and above, having Bishop score below 5, normal non-stress test (NST) at birth, normal oxytocin challenge test (OCT), lack of uterine contractions. Exclusion criteria included: contraindication of misoprostol or oxytocin, fetal macrosomia, polyhydramnios, placenta previa or abruption, meconial, vaginal bleeding, intrauterine growth restriction, non-cephalic presentation, and narrow pelvis.
- •Exclusion criteria are: contraindication of misoprostol or oxytocin, fetal macrosomia, polyhydramnios, placenta previa or abruption, meconial, vaginal bleeding, intrauterine growth restriction, non-cephalic presentation, and narrow pelvis.
- •Then need for cesarean section and fetal heart rate changes will be compared between two groups.
排除标准
- 未提供
研究者
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