TCTR20190415001Enrolling By Invitation4 期
Comparison of different dosage of oxytocin for initiating uterine contraction during cesarean delivery: A randomized, double-blind, controlled, non-inferiority trial
适应症
试验速览
- 阶段
- 4 期
- 状态
- Enrolling By Invitation
- 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 40 Years（—）
- 性别
- Female
入选标准
- •ASA physical status class II
- •singleton pregnancy
- •gestational age 37-42 weeks
- •patients were planned for cesarean delivery
- •patients were planned for spinal anesthesia
排除标准
- •failed or inadequate spinal anesthesia
- •high risk of uterine atony (macrosomia, twins, chorioamnionitis, polyhydramnios, myoma uteri)
- •previous uterus surgery (except cesarean section)
- •high risk of postpartum hemorrhage (placenta previa, history of previous postpatum hemorrhage, coagulopathy, thrombocytopenia, PIH)
- •contraindication of spinal anesthesia
- •allergy to oxytocin
- •refuse to be volunteer
研究者
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