IRCT20091010002558N7已完成1 期
Effect of prophylactic intravenous tranexamic acid on blood loss after cesarean delivery
Ghoum University of Medical Sciences0 个研究点目标入组 44 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 44
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 35 years（—）
- 性别
- Female
入选标准
- •Inclusion criteria included age 18-35 years, single pregnancy, cesarean delivery, blood pressure less than 140 over 90, no history of thromboembolism and coagulation disease, no uterine myoma, no IUFD fetus, no decolonization and no history or Active heart, liver and kidney diseases
排除标准
- •During cesarean section, if placental adhesions such as placenta, increta and percorta are observed, individuals will be excluded.
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