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临床试验/CTIS2023-504504-28-00
CTIS2023-504504-28-00进行中(未招募)1 期

The Direct Oral Anticoagulation versus Vitamin K Antagonist after Cardiac Surgery (DANCE) Trial - 2020.12.18

Hamilton Health Sciences Corporation0 个研究点目标入组 6,215 人开始时间: 2023年8月1日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
6,215

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 至 65+(—)
性别
All

入选标准

  • Age =18 years at the time of enrolment, Open heart surgery in the last 10 days, Atrial fibrillation requiring anticoagulation (including pre-existing or post-operative atrial fibrillation), Informed consent from either the patient or a substitute decision-maker.

排除标准

  • Mechanical valve replacement, Previously enrolled in this trial, Follow-up not possible, History of moderate or severe rheumatic valvular lesion (stenosis or regurgitation) that is not corrected during index cardiac surgery, Antiphospholipid syndrome (triple positive), Severe renal failure (Cockcroft-Gault equation; creatinine clearance <15 ml/min), Known significant liver disease (Child-Pugh classification B and C), Left ventricular thrombus, Ongoing bleeding, hemorrhagic disorders, or bleeding diathesis, Known contraindication for any direct oral anticoagulant or vitamin K antagonist, Women who are pregnant, breastfeeding, or of childbearing potential, Surgery including left ventricular assist device implantation or cardiac transplantation

研究者

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