CTRI/2017/07/009011尚未招募3 期
Effect of prophylactic use of tranexemic acid in post partum blood loss after normal vaginal delivery
AFMC0 个研究点目标入组 273 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 273
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
入选标准
- •Age > 20 yrs
- •Term pregnancies >37 wks
- •Singleton pregnancies
- •Planned vaginal deliveries
排除标准
- •Age <19 and >35 yrs
- •Pre eclampsia,multiple pregnancy,placental abnormalities
- •Instrumental deliveries
- •Any cardiovascular, renal, liver disorders
- •Any hematological , hemorrhagic disorders
- •H/o venous or arterial thrombosis
- •H/o use of LMWH or antiplatelet drugs
研究者
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