TCTR20161104004招募中4 期
Efficacy of tranexamic acid for reducing postpartum blood loss after vaginal delivery : a randomized control trial, double blind.
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- one
- 入组人数
- 150
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 0 N/A (No limit)（—）
- 性别
- Female
入选标准
- •Age >18 years
- •Normal delivery
- •Gestational age > 36 week
排除标准
- •-History of venous thrombosis (deep vein thrombosis and or pulmonary embolism)
- •or arterial thrombosis (angina pectoris, myocardial infarction, stroke)
- •-History of epilepsy or seizure
- •-Underlying disease cardiovascular,renal,liver disorders,Autoimmune disease
- •-Abnormal placenta : Placenta previa, Abnormally invasive placenta (placenta accreta/increta/percreta), Abruptio placenta 

- •-Preeclampsia with or without severe feature, Eclampsia,HELLP syndrome 

- •-Multiple pregnancy
- •-Vaccuum extraction, Forcep extraction 

- •-History of maternal use LMWH or anti platelet agents 1 week before delivery.
研究者
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