ACTRN12613001269729已完成2 期
Randomized clinical trial between two protocols of oral misoprostol for induction of labor
Abdulrahim Rouzi.0 个研究点目标入组 152 人开始时间: 2013年11月18日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 152
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 45 Years（—）
- 性别
- Female
入选标准
- •1.Singleton live pregnancy for induction of labor.
- •2.At or more than 34 weeks of gestation
- •3.Bishop score less than or equal to 6.
- •4.Intact membranes.
- •5.Cephalic presentation.
- •6.Reassuring fetal heart pattern.
排除标准
- •1. Hypersensitivity to misoprostol
- •2. Previous C/S or other uterine surgery.
- •3. Severe PIH (abnormal LFT’s, protein>1g/day, BP= 160/100).
- •4. Para 4 and more.
- •5. Multiple gestation.
- •6. Uterine contractions.
- •7. Significant maternal cardiac, renal , or liver disease.
研究者
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