CTRI/2021/02/031360尚未招募未知
Evaluation of blood loss during active management of third stage of labour with and without tranexamic acid
Gamidi Anusha0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
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 > 19 years and < 40 years
- •2)Spontaneous vaginal delivery
- •3)Induced vaginal delivery
- •4)Assisted vaginal delivery
- •5)Term > 35 weeks of gestation
- •6)Singleton pregnancy
排除标准
- •1)History of venous (deep vein thrombosis and/or pulmonary embolism) or arterial (angina pectoris,myocardial infarction, stroke) thrombosis
- •2) History of epilepsy or seizure
- •3) Any known cardiovascular, renal, or liver disorders
- •4)History of Autoimmune disease
- •5) History of Sickle cell disease
- •6) History of Severe hemorrhagic disease
- •7) Placenta previa
- •8)Abnormally invasive placenta (placenta accreta/increta/percreta)
- •9) Abruptio placentae
- •10) Eclampsia, HELLP syndrome
- •11) Multiple pregnancy
- •12) In utero fetal death
- •13) Administration of low-molecular-weight heparin or antiplatelet agents during the week before delivery
- •14)PROMâ??patients referred from periphery with PROM were excluded as the chances of chorioamnionitis were more due to repeated internal examinations
- •15)Prolonged and obstructed labour
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