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

Not Applicable
Completed
Conditions
Stroke
Atrial Fibrillation
Registration Number
NCT02261766
Lead Sponsor
Herlev Hospital
Brief Summary

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

Detailed Description

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

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • 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
Exclusion Criteria
  • earlier diagnose of atrial fibrillation
  • pacemaker or ICD device
  • stroke induced by trauma, infection or surgery procedure
  • carotid stenosis of more than 60%

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Atrial fibrillation detection rate on Thumb-ECG1 month
Secondary Outcome Measures
NameTimeMethod
Time to detection of atrial fibrillation on holter5 days
Atrial fibrillation detection rate on holtermonitoring5 days
Time to detection af atrial fibrillation on thumb-ECG30 days

Trial Locations

Locations (1)

Department of Neurology, Herlev Hospital

🇩🇰

Herlev, Denmark

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