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Clinical Trial Summary

The present study aims to investigate whether care improvement in patients after catheter ablation/cardioversion compared with standard care can be realized by using a digital eHealth platform with connected mobile sensors through early detection of atrial fibrillation recurrence and patient empowerment.


Clinical Trial Description

The main objective of the study is to compare the reliability of detection of atrial fibrillation of 2 measurement methods or protocols in terms of earliest possible detection: (1) digital eHealth platform with tethered 1-lead ECGs vs (2) standard-of-care long-term ECG. In addition, the quality of the acquired ECGs with both protocols will be compared by physician reporting based on the number of false positive abnormal findings as well as possible effects of using different mobile 1-lead ECGs. Secondary goals are the collection of data on patient adherence (e.g., reliability of performing recommended actions such as measuring ECGs, blood pressure and body weight, and taking medications), on the course of the disease, and on the use of the health care system. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05375877
Study type Interventional
Source iATROS GmbH
Contact Paul Weyh
Phone +49 176 856 23 142
Email paul.weyh@i-atros.com
Status Recruiting
Phase N/A
Start date February 3, 2022
Completion date July 31, 2024

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