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Clinical Trial Summary

To learn in a general Cardiac Resynchronization Therapy Defibrillators (CRT-D) population, which optimization techniques are used and how effective they are. It will compare 12-month response rates among different optimization methods and characterize which selected subject subgroups achieve better response than others. A subset of SMART Registry subjects will contribute to the NG4 Post Market Clinical Follow Up (PMCF) Cohort whose objective is collecting data on the NG4 CRT-D features and device usage in a real world setting and monitor long term safety associated with these devices to support CE Mark.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03075215
Study type Observational [Patient Registry]
Source Boston Scientific Corporation
Contact
Status Completed
Phase
Start date April 14, 2017
Completion date November 15, 2021

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