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Clinical Trial Summary

The BIO|GUARD-MI study investigates whether continuous arrhythmia monitoring and the consequent treatment after detected arrhythmias in patients after myocardial infarction with preserved cardiac function, but other risk factors, decreases the risk of major adverse cardiac events.


Clinical Trial Description

Patients randomized to the BioMonitor arm will receive an implantable cardiac monitor (ICM; BioMonitor) with remote monitoring function (Home Monitoring®). If the device detects and reports an arrhythmia, patients will be appropriately examined and treated. Patients randomized to the control arm will receive best proven treatment, but no implantable cardiac monitor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02341534
Study type Interventional
Source Biotronik SE & Co. KG
Contact
Status Completed
Phase N/A
Start date August 7, 2015
Completion date November 3, 2021

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