IRCT20140420017365N4已完成3 期
Evaluation Efficacy of Tranexamic acid in decreasing blood loss in cesarean delivery
Oroumia University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 100
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
- •Candidate for Elective Singleton Cesarean section
- •Having adequate prenatal care.
- •Complete the form of informed consent
- •Age range 18-45 years
排除标准
- •Patients do not accept to participate in the study
- •They have anemia and bleeding diseases or serious medical or surgical diseases
- •Sensitivity to Tranexamic acid
- •Fetal macrosomia
- •Thromboembolism Score(V.T.E. scoring)=3
- •Placental Abruption , placenta parvia and abnormal placental adherence
- •Uterine myoma more than 5 cm
- •Polyhydramnios
- •Multi-fetus pregnancy
- •Use of Anticoagulant such as enoxaparin or heparin
- •Severe pregnancy complications such as preeclampsia
- •Long-term hospitalization more than 3 days before cesarean section
研究者
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