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Inappropriate Shock Reduction wIth PARAD+ Rhythm DiScrimination — ISIS-ICD  

Tachycardia Clinical Trial

Official title:
Inappropriate Shock Reduction wIth PARAD+ Rhythm DiScrimination

Clinical Trial Summary

ISIS- ICD study has been designed to evaluate the impact of PARAD+ algorithm on inappropriate shocks, in a general population implanted for primary or secondary prevention with a dual or tri chamber device at one year follow-up

Clinical Trial Description

The primary endpoint is to demonstrate that 95% of patients implanted with PARAD+ algorithm are free from inapproporiate shock compared to 92.5% in general ICD population. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01410552
Study type Interventional
Source MicroPort CRM
Contact
Status Completed
Phase N/A
Start date October 2011
Completion date February 2016
View Details
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