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Clinical Trial Summary

The investigators will evaluate the diagnostic yield of the new AliveCor device versus a 12 lead ECG when used simultaneously to detect cardiac arrhythmia


Clinical Trial Description

The investigators are planning to record 250 pre-defined abnormal ECGs (50 each of atrial fibrillation, atrial flutter, pre-excitation, ventricular tachycardia, , supraventricular tachycardia) and 150 control ECGs (100 sinus rhythm, 50 sinus tachycardia) using both the AliveCor Smartphone device and a 12-lead ECG. All 400 ECGs will then be read by 3 blinded reporters - a Consultant Electrophysiologist, a Consultant General Cardiologist and a General Practitioner. The output of the AliveCor automatic detection algorithm will also be recorded as a fourth reporter. The screening characteristics of all 4 reporters using the AliveCor device vs the definitive 12 lead ECG will be analysed and compared. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03996954
Study type Interventional
Source Blackpool Teaching Hospitals NHS Foundation Trust
Contact Khalid Abozguia, Ph.D.
Phone 00441253957780
Email k.abozguia@nhs.net
Status Recruiting
Phase N/A
Start date October 8, 2018
Completion date October 7, 2020

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