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Clinical Trial Summary

All patients having an implantable cardiac defibrillator (ICD) implanted and having follow-up at the Cantonal Hospital Lucerne (LUKS), the investigator center, are included in this retrospective ICD lead registry from 2006 onwards. Data is collected prospectively from december 2016 onwards. After certain ICD-leads tended to fail early the investigators aimed for a registry monitoring our patient population with defibrillator leads and evaluating their long-term performance.


Clinical Trial Description

All patients having an ICD implanted and having follow-up at the investigators center are included in this retrospective ICD lead registry from 2006 onwards. Data is collected prospectively from december 2016 onwards. After certain ICD-leads tended to fail early the investigators aimed for a registry monitoring our patient population with defibrillator leads and evaluating their long-term performance.

The following parameters will be measured during regular clinical controls: electronic impedances, threshold values, sensing values, battery performance, inadequate/adequate shock release und software problems ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03521050
Study type Observational [Patient Registry]
Source Luzerner Kantonsspital
Contact Richard Kobza, MD
Phone +41412055144
Email richard.kobza@luks.ch
Status Recruiting
Phase
Start date December 2016
Completion date December 2026

See also
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Completed NCT01006746 - Observational Study of Patient Comprehension, Perception, Fears and Appreciation Following Home-Monitoring Implementation N/A