IRCT20191208045653N1招募中早期 1 期
The effect of outpatient sublingual misoprostol 25 µg and oral misoprostol 50 µg on reducing post-term pregnancy and induction success and evaluation of maternal and fetal outcomes: a double-blind clinical trial
适应症
试验速览
- 阶段
- 早期 1 期
- 状态
- 招募中
- 入组人数
- 140
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 50 years（—）
- 性别
- Female
入选标准
- •Maximum gestational age of 40 weeks
- •pregnant women
- •Prime Grave
- •Single pregnancy
- •Cephalic display
- •Having normal amniotic fluid (AFI greater than or equal to 5 cm)
- •Bishop Score less than 8
- •Maternal age between 18 and 40 years
排除标准
- •History of medical and midwifery disease
- •Preeclampsia
- •History of stillbirth
- •Opt out of the study
- •Improper use of medication
研究者
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