IRCT201204079399N1已完成2 期
A placebo-controlled clinical trial to assess efficacy of tranexamic acid in reducing hemorrhage after vaginal delivery
Vice chancellor for research ,Kashan University of Medical Sciences0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 200
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
- 15 years 至 50 years（—）
- 性别
- Female
入选标准
- •1- inclusion criteria:
- •- women with term, singleton pregnancy candidate for the first vaginal delivery
- •-No history of sever medical complications involving the heart,brain ,kidney
- •- No history of allergy to tranexamic acid
- •-No history of visual problem
- •-No history of sever pregnancy complications such as preeclampsia
- •-No history of thromboembolic events
- •2- exclusion criteria:
- •-patient avoidance
- •-placenta abruption
排除标准
- 未提供
研究者
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