ACTRN12615000312549已完成4 期
Efficiency and safety of preoperative Tranexamic acid compared to a placebo in reducing perioperative blood loss in women undergoing elective cesarean section
Ahmed Maged0 个研究点目标入组 200 人开始时间: 2015年4月2日最近更新:
试验速览
- 阶段
- 4 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
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 19 Years 至 41 Years（—）
- 性别
- Female
入选标准
- •full-term singleton pregnancies underwent elective lower segment caesarean section
排除标准
- •1.prolonged CS (> 90 min according to anesthetic record), 2.anemic patients (Hb < 9 gm %),
- •3.presence of maternal medical disorder (e.g. cardiac, renal, hepatic & coagulopathies) or
- •4.history of thrombo-embolic events.
- •5.known allergy to TA.
- •6.Patients with increased risk for obstetric hemorrhage (e.g. antepartum hemorrhage, abnormal placentation, previous history of uterine atony & postpartum hemorrhage, polyhydramnios & uterine fibroids).
研究者
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