IRCT20201022049108N1已完成3 期
Evaluation of the Efficacy of Rectal or Sub-linguinal Misoprostol concomitant with Oxytocin for Prevention of Postpartum Hemorrhage in women with preeclampsia
Karaj University of Medical Sciences0 个研究点目标入组 128 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 128
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 45 years（—）
- 性别
- Female
入选标准
- •ALL pregnant mothers with severe pre-eclampsia who referred to the Shahi Kamali educational center in the study period
- •Hospitalization for C-section
- •Gestational age over 35 weeks
- •Having a healthy and alive fetus
- •Cephalic fetus
- •A maximum of 2 previous cesarean sections
- •Complete removal of the placenta after cesarean section
- •The age of 18-45 years
排除标准
- •Mothers with coagulation disorders
- •History of maternal blood disorders
- •Chronic hypertension
- •Placental adhesion such as placenta previa and ecrta
- •Placental abruption (overt and covert)
- •Complications or emergency during surgery
- •Mild pre-eclampsia
- •Abnormal placenta
- •History of uterine rupture
- •High bleeding risk
- •Indication for hysterectomy or T
研究者
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