ChiCTR2100047385已完成Unknown
A Randomized control study of titrated and static oral misoprostol solution for induction of labor at term
Dr Barbie Sharma1 个研究点 分布在 1 个国家目标入组 264 人开始时间: 2017年11月1日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 264
- 试验地点
- 1
- 主要终点
- Induction to delivery time
研究概览
简要总结
Our objective in this study was to evaluate effectiveness and safety of titrated oral misoprostol solution in comparison with static-dose oral misoprostol solution for induction of labor at term.
研究设计
- 研究类型
- Interventional
- 主要目的
- 随机平行对照
- 盲法
- None
入排标准
- 年龄范围
- 18 至 40（—）
- 性别
- Female
入选标准
- •Singleton live pregnancy;
- •>=37 weeks gestation;
- •Cephalic presentation;
- •Reactive NST
- •Modified Bishops score <=6.
排除标准
- •Hypersensitivity to misoprostol;
- •Uterine scar due to previous cesarean section or other uterine surgery;
- •Grand multipara;
- •Multiple gestations;
- •High risk pregnancies preeclampsia with severe features significant maternal cardiac, renal, liver disease;
- •Any contraindication to induction and vaginal delivery e.g. cephalopelvic disproportion, malpresentation, fetal compromise and ante partum hemorrhage;
- •Intrauterine fetal demise.
研究组 & 干预措施
titrated oral misoprostol solution versus static-dose oral misoprostol solution
titrated oral misoprostol solution versus static-dose oral misoprostol solution
结局指标
主要结局
Induction to delivery time
次要结局
未报告次要终点
研究者
研究点 (1)
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