IRCT201405313485N4已完成2 期
The effect of tranexamic acid on blood loss during and after cesarean in women who candidate for cesarean section delivery by clinical trial study
Vice Chancellor for Research, Guilan University of Medical Sciences, Rasht, Iran0 个研究点目标入组 80 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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
- 135 years 至 137 years（—）
- 性别
- Female
入选标准
- •Primiparas and multiparas females with singleton pregnancy during the gestational ages of 37 to 40 weeks who are going to be delivered by cesarean section through fannenstiel’s incision and spinal anesthesia
- •Non-inclusion criteria: Patients with problem of heart, liver and kidney; hematologic or rheumatologic problems; history of thyroid disease; abnormal placental; severe preeclampsia; macrosomia; severe anemia; problematic obstetric history
- •Exclusion criteria: allergy to Tranexamic acid
排除标准
- 未提供
研究者
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