ACTRN12616000522415终止4 期
Cervical Ripening Using Misoprostol vs Dinoprostone: A randomised, triple-blinded, interventional study comparing safety and efficacy in primiparous women
适应症
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 208
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
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •1) Pregnant women between 37+0 and 41+4 weeks gestation
- •2) Having first baby
- •3) Induction of labour deemed medically indicated
- •4) Bishops score less than or equal to 4
- •5) age >=18
- •6) BMI <50 at booking visit
排除标准
- •1) Active labour
- •2) Ruptured membranes
- •3) Non-cephalic presentation
- •4) Previous caesarean section or other uterine surgery
- •5) Unexplained vaginal bleeding >24 weeks gestation
- •6) Suspected or known chorioamnionitis
- •7) Suspected or known fetal compromise (abnormal antenatal fetal heart rate pattern, ultrasound showing fetal growth <10th centile, oligohydramnios, polyhydramnios, abnormal dopplers)
- •8) Unable to read or speak English without the aid of an interpreter
研究者
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