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Clinical Trial Summary

The proposed study is designed to characterize the safety and efficacy of a new extravascular implantable cardioverter defibrillator (ICD) system in humans.


Clinical Trial Description

The study will recruit male and female adult subjects that meet all of the inclusion criteria and none of the exclusion criteria. All subjects will be indicated to receive an ICD. The EV ICD system will be implanted and the subjects will be followed for at least 3 months following implantation of the system. Subjects will be exited after follow-up is completed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03608670
Study type Interventional
Source Medtronic Cardiac Rhythm and Heart Failure
Contact
Status Completed
Phase N/A
Start date July 17, 2018
Completion date November 15, 2023

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