IRCT20171111037374N1已完成2 期
Comparing the Effect of Oral Misoprostol and Intravenous Oxytocin on Labor Induction in pregnant women
Fasa University of Medical Sciences0 个研究点目标入组 140 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
- 发起方
- 入组人数
- 140
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 no limit（—）
- 性别
- Female
入选标准
- •Gestational age more than 42 weeks
- •first and second pregnancy
- •women over 18 years old
- •singleton pregnancy,
- •cervical closure (Bishop score greater than six)
排除标准
- •Multiple pregnancies
- •need for immediate cesarean section
- •history of uterine scarring
- •placenta previa
- •vaginal bleeding more than normal postpartum bleeding
- •heart, liver and kidney diseases
- •history of sensitivity to Oxytocin, Misoprostol or prostaglandin analogues
- •severe congenital anomalies in the fetus.
研究者
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