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Experience From the Italian S-ICD Registry — ELISIR  

Cardiac Arrest Clinical Trial

Official title:
Experience From the Long-term Italian Subcutaneous Implantable Cardioverter Defibrillator Registry (ELISIR)

Clinical Trial Summary

The purpose of this registry is to collect data on implant parameters, early, mid and long-term clinical effectiveness of Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) therapies in order to better understand how to improve the clinical care of patients and effectiveness of S-ICD therapies.

Clinical Trial Description

ISIR is an observational, multicentric registry designed to collect implant and follow-up data of consecutive patients implanted with Subcutaneous Implantable Cardioverter Defibrillator (S-ICD). A number of about 10 enrolling centers is estimated with an overall number of 400 patients. A minimal follow-up of 6 months is required before analyzing clinical outcomes. The data analysis will focus on implant outcomes and early, mid and long-term effectiveness of S-ICD therapies and safety. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04373876
Study type Observational [Patient Registry]
Source Luigi Sacco University Hospital
Contact
Status Recruiting
Phase
Start date January 1, 2020
Completion date December 2022
View Details
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