Evaluation of 5 Days Holter and 30 Days Thumb-ECG for Detection of Atrial Fibrillation in Stroke Patients
Not Applicable
Completed
- Conditions
- StrokeAtrial 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
Name Time Method Atrial fibrillation detection rate on Thumb-ECG 1 month
- Secondary Outcome Measures
Name Time Method Time to detection of atrial fibrillation on holter 5 days Atrial fibrillation detection rate on holtermonitoring 5 days Time to detection af atrial fibrillation on thumb-ECG 30 days
Trial Locations
- Locations (1)
Department of Neurology, Herlev Hospital
🇩🇰Herlev, Denmark