Skip to main content
Clinical Trials/NCT02261766
NCT02261766
Completed
Not Applicable

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

Herlev Hospital1 site in 1 country100 target enrollmentAugust 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
Herlev Hospital
Enrollment
100
Locations
1
Primary Endpoint
Atrial fibrillation detection rate on Thumb-ECG
Status
Completed
Last Updated
10 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
August 2012
End Date
June 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Karsten Overgaard

Medical Doctor

Herlev Hospital

Eligibility Criteria

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%

Outcomes

Primary Outcomes

Atrial fibrillation detection rate on Thumb-ECG

Time Frame: 1 month

Secondary Outcomes

  • 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)

Study Sites (1)

Loading locations...

Similar Trials