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Clinical Trial Summary

Prospective, non-randomized, multi-center study designed to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers


Clinical Trial Description

The purpose of this study is to quantify patient preferences pertaining to risks and features of conventional transvenous pacemakers and leadless pacemakers. The preference study is designed to elicit patient preferences for risks and features that vary between a dual chamber leadless pacemaker system and a dual chamber transvenous pacemaker system, to quantify their relative importance. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05327101
Study type Observational [Patient Registry]
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date March 28, 2022
Completion date June 13, 2023

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