Clinical Trials Directory

Trials / Completed

CompletedNCT02261766

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

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Herlev Hospital · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
DEVICEHolter monitoring and Thumb ECG5 days holtermonitoring and 30 days 30 seconds twice daily thumb ECG recording

Timeline

Start date
2012-08-01
Primary completion
2015-02-01
Completion
2015-06-01
First posted
2014-10-10
Last updated
2015-06-24

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT02261766. Inclusion in this directory is not an endorsement.

Evaluation of 5 Days Holter and 30 Days Thumb-ECG for Detection of Atrial Fibrillation in Stroke Patients (NCT02261766) · Clinical Trials Directory