LUKS-Leads Registry on Long-term Performance of ICD Leads

Luzerner Kantonsspital

Status: Enrolling

Conditions: Defibrillators; Electrical Shock

Treatments: Device: defibrillator lead

Study type: Observational

Funder types: Other

Identifiers

NCT03521050

2016-02002

Details and patient eligibility

About

All patients having an implantable cardiac defibrillator (ICD) implanted and having follow-up at the Cantonal Hospital Lucerne (LUKS), the investigator center, are included in this retrospective ICD lead registry from 2006 onwards. Data is collected prospectively from december 2016 onwards. After certain ICD-leads tended to fail early the investigators aimed for a registry monitoring our patient population with defibrillator leads and evaluating their long-term performance.

Full description

All patients having an ICD implanted and having follow-up at the investigators center are included in this retrospective ICD lead registry from 2006 onwards. Data is collected prospectively from december 2016 onwards. After certain ICD-leads tended to fail early the investigators aimed for a registry monitoring our patient population with defibrillator leads and evaluating their long-term performance.

The following parameters will be measured during regular clinical controls: electronic impedances, threshold values, sensing values, battery performance, inadequate/adequate shock release und software problems

Enrollment: 1,000 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• all patients being implanted with a Defibrillator lead from 2006 onwards

Exclusion criteria

• documented refusal of data collection for scientific purposes

Trial design

1,000 participants in 1 patient group

implanted defibrillator lead

Description:

patients having an ICD implanted and having follow-up at the investigators center

Treatment:

Device: defibrillator lead