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Clinical Trial Summary

Understanding the clinical practice of treatment of cardiac rhythm disorders all over the world and understanding the clinical outcomes of the treatment with its cardiac rhythm products in real world patient population is essential for Medtronic to be able to effectively develop new products and adjust existing products. In addition Medtronic is committed to monitor the safety of its products throughout the entire life cycle to ensure maximum product reliability.

The Panorama 2 registry will enable Medtronic to increase data collection of clinical practice with Medtronic implantable Cardiac Rhythm and Disease Management (CRDM) devices in various regions across the world and on product reliability of its CRDM devices.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01723566
Study type Observational
Source Medtronic Bakken Research Center
Contact
Status Completed
Phase N/A
Start date July 25, 2012
Completion date October 31, 2016

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