IRCT20230227057554N1尚未招募3 期
Investigating the incidence of postpartum hemorrhage in high-risk pregnant women who underwent cesarean section after the prophylactic administration of misoprostol, metrogen, and oxytocin compared to oxytocin alone
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 240
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
- •Singleton term pregnant women who have an indication for termination of pregnancy (37-40 weeks).
- •Have an indication for an elective cesarean section.
- •At least one risk factor for postpartum bleeding (such as polyhydramnios, multiparity, having a history of postpartum bleeding, macrosomia, and anemia).
排除标准
- •Emergency cesarean section
- •Abnormal fetal heartbeat
- •Vaginal bleeding
- •Person with unexpected bleeding during the surgery
- •Severe anemia (hemoglobin less than 8 mg/dL) before surgery
- •Advanced underlying diseases
- •History of coagulation disorders
- •Low-lying placenta, decolman or accreta previa
- •Reaction history to the drugs
研究者
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