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临床试验/NCT02261766
NCT02261766已完成不适用

Detection of Atrial Fibrillation, -Evaluation of 5 Days Holter and 30 Days Thumb-ECG for Detection of Atrial Fibrillation in Stroke Patients

Herlev Hospital2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
2
主要终点
Atrial fibrillation detection rate on Thumb-ECG

研究概览

简要总结

This study will compare the two methods 5 days holtermonitoring and 30 days thumb electrocardiogram for detection of atrial fibrillation in stroke patients

详细描述

Patients with a newly stroke will be examined with both 5 day holter monitoring and 30 days thumb ECG at the same time. The detection rates of the two methods will be compared

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • stroke or TIA within the last 3 months verified by a CT or a MR scan or unequivocal symptoms and old infarcts visualised on CT or MR
  • age 65 or above
  • patients able to handle the thumb-ECG
  • written informed consent

排除标准

  • earlier diagnose of atrial fibrillation
  • pacemaker or ICD device
  • stroke induced by trauma, infection or surgery procedure
  • carotid stenosis of more than 60%

结局指标

主要结局

Atrial fibrillation detection rate on Thumb-ECG

时间窗: 1 month

次要结局

  • Atrial fibrillation detection rate on holtermonitoring(5 days)
  • Time to detection of atrial fibrillation on holter(5 days)
  • Time to detection af atrial fibrillation on thumb-ECG(30 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Karsten Overgaard

Medical Doctor

Herlev Hospital

研究点 (2)

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