IRCT20200421047152N4尚未招募3 期
Safety and efficacy of cervical administration of misoprostol in induction of labor in mothers with unripe cervix and term pregnancy compared to vaginal and sublingual administration: a randomized clinical trial.
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 123
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 40 years（—）
- 性别
- Female
入选标准
- •Women aged 18-40 years
- •Singleton pregnancy
- •Cephalic presentation
- •Gestational age more than 37 weeks
- •Appropriate pelvic examination
- •Intact membranes
- •Fetal weight between 90-10th percentile estimated by ultrasound
- •ishop score less than or equal to 6
排除标准
- •Birth history equal to or more than 3
- •Blood pressure equal to or greater than 140/90 mmHg
- •Proteinuria or preeclampsia
- •Getational diabetes
- •Unreliability of fetal heart trace or any fetal distress
- •Polyhydramnios or oligohydramnios
- •The possibility of fetal macrosomia
- •Intrauterine fetal death
- •Previous history of uterine surgery
- •Placenta previa
研究者
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