IRCT2012102910068N2已完成早期 1 期
comparison the effect of oral Misoprostol versus Oxytocin on labor augmentation in pregnant women
Shahid Beheshti University of Medical Science0 个研究点目标入组 250 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 早期 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 250
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
- 16 years 至 45 years（—）
- 性别
- Female
入选标准
- •pregnancy between 36 and 42 weeks of gestation; a live singleton fetus in cephalic presentation; no history of uterine surgery; spontaneous onset of active labor with regular contractions; an effaced cervix dilated between 3 cm and 9 cm; a reassuring fetal heart rate (FHR) pattern.
- •Exclusion criteria:
- •nonreassuring FHR pattern; parity greater than five; any contraindication to labor or vaginal delivery or both; epidural analgesia; significant maternal cardiac; renal or hepatic disease; hypersensitivity to misoprostol or prostaglandin analogues.
排除标准
- 未提供
研究者
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