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Experience From the Italian S-ICD Registry

NCT04373876 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2021-04-13

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Subcutaneous Implantable Cardioverter Defibrillator

Patients implanted with a totally subcutaneous defibrillator system

Sponsors & Collaborators

  • Luigi Sacco University Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-01
Primary Completion
2022-12-31
Completion
2022-12-31
FDA Device
Yes

Countries

  • France
  • Germany
  • Italy
  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04373876 on ClinicalTrials.gov