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临床试验/NCT03570060
NCT03570060已完成不适用

Stepwise Screening for Silent Atrial Fibrillation After Stroke

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 264 人开始时间: 2018年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
264
试验地点
1
主要终点
Diagnosis of atrial fibrillation during continuous monitoring in a Stroke unit within six months of stroke.

研究概览

简要总结

The main hypothesis of this work is that an approach combining clinical parameters and biomarker assays could improve the understanding and prediction of the occurrence of silent atrial fibrillation (AF) in the acute phase after stroke. In this prospective work, the investigators will rely on the Dijon Stroke Registry, which collects extensive clinical data for each patient hospitalized for a stroke. As part of this registry, patients are seen 6 months after stroke to assess their clinical status. This clinical follow-up will allow us to judge the evolution of the AF diagnosed during the acute episode at a distance.

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

  • Patient who had an ischemic stroke defined according to WHO criteria and hospitalized in the Stroke Unit at the Dijon University Hospital.
  • Patient 18 years of age and older
  • Patient who has given oral consent

排除标准

  • Person not affiliated to a national health insurance scheme
  • Protected adult
  • Pregnant or breastfeeding woman
  • Patient refusing to participate in the study
  • Transfer planned after the stay in the Stroke Unit to a department outside the Dijon University Hospital, not allowing for the long term screening with an external ECG monitor
  • History of atrial fibrillation or atrial flutter
  • Patient wearing a pacemaker or defibrillator with an atrial lead

结局指标

主要结局

Diagnosis of atrial fibrillation during continuous monitoring in a Stroke unit within six months of stroke.

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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