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Clinical Trial Summary

The purpose of the study is to compare standard, single chamber transvenous ICD to sub-cutaneous ICD in occurrence of perioperative and long term device related complications and failed appropriate clinical shocks and arrhythmic death.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02881255
Study type Interventional
Source Population Health Research Institute
Contact
Status Completed
Phase N/A
Start date February 22, 2017
Completion date February 10, 2022

See also
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