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Clinical Trial Summary

Observational study on long PR interval using the SafeR mode in bradycardia patients.


Clinical Trial Description

This observational trial aims to study the evolution of the PR interval in patients implanted with a dual chamber pacemaker with the SafeR mode. The investigators will assess the prevalence and the incidence of PR lengthening and the investigators will study the long PR interval management by physicians, depending on the data embedded in the pacemaker. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02586480
Study type Observational [Patient Registry]
Source LivaNova
Contact
Status Completed
Phase N/A
Start date April 2012
Completion date December 2015

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