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临床试验/NCT05011981
NCT05011981进行中(未招募)不适用

Hemostatic Activity Following Left Atrial Appendage Occlusion

University of Aarhus1 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2021年10月11日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
135
试验地点
1
主要终点
Change in coagulation activity

研究概览

简要总结

The primary objective of this study is to prospectively investigate hemostatic activity following transcatheter left atrial appendage occlusion (LAAO).

详细描述

This is a prospective cohort study of patients undergoing transcatheter LAAO at Aarhus University Hospital. Hemostatic consequences following device implantation will be evaluated using blood samples collected pre- and post-procedurally, and serially during three months follow-up in 135 LAAO patients. Platelet function and characteristics, overall activation of the extrinsic coagulation pathway and the intrinsic contact activation pathway, as well as endothelial response to implantation, will be assessed through a wide range of biochemical analyses. Patients will serve as their own controls, with a final control blood sample collected at three-months follow-up.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years
  • Atrial fibrillation (paroxysmal, persistent, or permanent)
  • Admitted and eligible for LAAO
  • Signed written consent

排除标准

  • Known hereditary bleeding disorders (i.e. Hemophilia A and B, Von Willebrand disease)
  • Platelet count < 75 x 109/ml

结局指标

主要结局

Change in coagulation activity

时间窗: 7 days, 14 days, 90 days

Coagulation activity as measured by prothrombin fragment 1+2

次要结局

  • Non-procedural bleeding events(7 days, 14 days, 90 days)
  • Additional measures of changes in coagulation and contact activation(7 days, 14 days, 90 days)
  • Radiographical evidence of device endothelization(7 days, 14 days, 90 days)
  • Change in platelet activity(7 days, 14 days, 90 days)
  • Change in endothelial activation and response(7 days, 14 days, 90 days)
  • Radiographically confirmed device-related thrombosis(7 days, 14 days, 90 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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