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Clinical Trial Summary

A randomized, open, mono-centric pilot study to investigate the influence of an innovative telemetric smartphone application on re-hospitalization and quality of life after cryoballoon pulmonary vein isolation in patients with paroxysmal atrial fibrillation.


Clinical Trial Description

The telemetric smartphone application includes a digitized medical record, a mobile ECG device and a 24-hour on call service by a cardiologist. The hypothesis is that the use of a telemetric smartphone application can reduce re-hospitalization in patients after cryoballoon pulmonary vein isolation. Secondary endpoints are quality of life measurements, health care cost calculations and recurrences of atrial fibrillation after ablation. All patients will undergo ablation and will be randomized into two groups: 1) conventional follow up with outpatient visits 6 and 12 months after ablation compared to 2) a structured follow up with the smartphone application, a mobile ECG device (patients will be able to send in as many ECGs as wanted), up to three phone calls with a cardiologist (24-hour on call service) as well as outpatient visits 6 and 12 months after cryo-ablation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03268707
Study type Interventional
Source Universitätsklinikum Hamburg-Eppendorf
Contact Melanie Gunawardene, MD
Phone 004940741054120
Email m.gunawardene@uke.de
Status Recruiting
Phase N/A
Start date July 15, 2017
Completion date June 30, 2021

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