IRCT2012061910068N1已完成早期 1 期
Induction and augmentation of labor with oral misoprostol versus oxytocin in term pregnancy: randomized controlled trial
Shahid Beheshti University of Medical Science0 个研究点目标入组 285 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 早期 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 285
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
- 14 years 至 40 years（—）
- 性别
- Female
入选标准
- •term pregnant women whom were candidate for vaginal delivery; gestational age of 38 to 42 weeks; birth weight of maximally 4000 grams; normal fetal heart rate; cephalic presentation; lack of uterine contractures; single pregnancy and Bishop Score of six and less.
- •The exclusion criteria were lack of satisfaction for incorporation in the study; having a positive history of uterine surgery including cesarean; intrauterine growth retardation (IUGR); oligohydramnios; placenta previa; umbilical cord prolapse; active herpes infection; symptoms of chorioamnionitis; hepatic or renal disease; non-reactive contraindications for prostaglandins use; contraindications for labor induction and idiopathic vaginal bleeding.
排除标准
- 未提供
研究者
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