NCT01070472已完成不适用
Efficacy and Safety of Titrated Oral Misoprostol Solution for Labor Induction at Term
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 250
- 试验地点
- 1
- 主要终点
- Rate of vaginal delivery within 24 hours
研究概览
简要总结
The purpose of this study is to determine whether a titrated solution of oral Misoprostol is safe and effective at inducing labor at term, regardless of Bishop Score.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 44 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •no contraindication to prostaglandins
- •no exposure to vaginal prostaglandins in the index pregnancy
排除标准
- •parity > 3
- •severe PIH: BP> 160/100, abnormal LFT's, proteinuria >1g/day
- •previous uterine surgery
- •regular uterine contractions
- •maternal age > 45
结局指标
主要结局
Rate of vaginal delivery within 24 hours
时间窗: 24 hours
次要结局
- Uterine hyperstimulation rate(24 hours)
研究者
Dr. debbie Robinson
Dr
University of Manitoba
研究点 (1)
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