TCTR20191230002Enrolling By Invitation3 期
Randomized trial comparing efficacy of 12.5 and 25 µg oral misoprostol 2 hourly for induction of labor
donthani hospital0 个研究点目标入组 160 人开始时间: 2019年12月30日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 160
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 0 N/A (No limit)（—）
- 性别
- Female
入选标准
- •women with singleton live pregnancy , Gestational age greater than or equal to 38 weeks , have indication of induction of labor , vertex presentation, normal fetal heart rate , Bishop score less than or equal to 6 point , intact membrane
排除标准
- •refuse participate in research , misoprostol allergy , previous cesarean section or myomectomy ,underlying disease such as heart, renal ,liver disease ,severe preeclampsia with severe feature , Grand multiparity ,regular uterine contraction , multifetal pregnancy , active genital tract disease , DFIU and fetal anomaly , estimate fetal weight more than 4000 grams
研究者
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