IRCT2014061412789N3已完成未知
A comparison of vaginal and oral dose of misoprostol for labor induction in post-term pregnancies
Vice Chancellor for Research, Kurdistan University of Medical Sciences0 个研究点目标入组 180 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
- 180
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 35 years（—）
- 性别
- Female
入选标准
- •Gestational age (GA) greater or equal to 40 weeks and 6 days with cephalic presentation and Bishop score greater than 4 and a height of 150 cm. Exclusion criteria included contraindications to receive misoprostol (allergies, asthma, Pelvic Inflammatory Disease, Acute Cerebrovascular Disease, Coronary Artery Disease, seizures) and also placenta previa , history of previous cesarean section or uterine surgery, Cephalopelvic Disproportion , Bishop score greater than 4, and abnormal vaginal bleeding.
排除标准
- 未提供
研究者
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