CTRI/2024/05/066737尚未招募4 期
Ideal time for administration of prophylactic tranexamic acid for reducing blood loss and preventing postpartum hemorrhage in cesarean delivery in a tertiary health care centre: A single-centre, double-blind, randomized controlled non-inferiority trial. - NI
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
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
- •a)Women undergoing elective or emergency LSCS.
- •b)Gestational age = 32weeks.
排除标准
- •a)History of previous thrombotic event or preexisting pro-thrombotic disease.
- •b)Any active or chronic cardiovascular disease except for hypertension.
- •c)Any chronic or active kidney disease or insufficiency.
- •d)Chronic or active liver disease.
- •e)Autoimmune disease.
- •f)Sickle cell disease.
- •g)Placenta accreta/increta/percreta.
- •h)Eclampsia, HELLP syndrome
- •i)Received antiplatelet drugs during the week before delivery.
- •j)Known allergy to tranexamic acid.
- •k)Women who develop PPH before cord clamping
研究者
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