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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-08-31

Study Completion Date

2015-06-30

Brief Summary

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

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Detailed Description

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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

Conditions

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Atrial Fibrillation Stroke

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Interventions

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Holter monitoring and Thumb ECG

5 days holtermonitoring and 30 days 30 seconds twice daily thumb ECG recording

Intervention Type DEVICE

Eligibility Criteria

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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%

Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No