CTRI/2021/05/033500已完成3 期
Effect of Intravenous Tranexamic Acid (TXA) In Addition To Active Management Of Third Stage Of Labour On Postpartum Blood Loss In Vaginal Delivery: A double Blinded , Randomized Controlled Trial - TAAPP-V Trial
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 641
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
- •1.Age > 18 years
- •2.Gestational age 34+0 weeks or more
- •3.Singleton pregnancy
- •4.Planned vaginal delivery
- •5.Available venous hemogram value in week before vaginal delivery
- •6.Signed informed consent to participate in study
排除标准
- •1. History of venous thrombosis: deep vein thrombosis, pulmonary embolism
- •2. History of arterial thrombosis: myocardial infarction, stroke
- •3. Any known cardiovascular, renal, or liver disorders
- •4. Autoimmune disease e.g. secondary APLA
- •5. Sickle cell disease
- •6. Severe haemorrhagic disease e.g.; VWD
- •7. Obstetric complications - multiple pregnancy, placenta previa, abruptio placentae, Abnormal invasive placenta (placenta accrete/ increta/ percreta), Eclampsia or HELLP (haemolysis elevated liver low platelet) syndrome, in utero fetal death
- •8.Administration of low-molecular weight heparin or antiplatelet agents in the week before delivery
- •9. History of Epilepsy or seizure
- •10. Active subarachnoid haemorrhage
- •11. Colour vision disturbances
- •12. Known hypersensitivity to tranexamic acid
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