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Austrian Wearable Cardioverter Defibrillator Registry

Indications for and Experience With the Wearable Cardioverter Defibrillator (WCD) - Austrian WCD Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02816047
Enrollment
450
Registered
2016-06-28
Start date
2014-11-30
Completion date
2022-03-31
Last updated
2021-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Sudden Cardiac Arrest, Sudden Death, Ventricular Dysfunction, Ventricular Fibrillation, Ventricular Tachycardia

Keywords

wearable cardioverter defibrillator, LifeVest, sudden death, defibrillator

Brief summary

Background: The wearable cardioverter defibrillator (WCD) is an established treatment option for patients at high risk for ventricular tachycardia / ventricular fibrillation (VT/VF), either in whom this risk may only be temporarily present, or in patients at high risk for sudden cardiac death (SCD) or after VT/VF in whom an implantable cardioverter defibrillator (ICD is currently not possible for other reasons (infection, recent MI \<40days, recent PCI/CABG \< 3months etc.). Methods: Comprehensive registry including all patients in Austria who received a WCD in 2010-2016.

Detailed description

Observational study to describe WCD indications, event rates, inappropriate shock rates and follow up (including ICD rate, shock rate, morbidity and mortality) in all Austrian WCD patients

Interventions

OTHERRegistry

Observational study to describe WCD indications, event rates, inappropriate shock rates and follow up (including ICD rate, shock rate, morbidity and mortality) in all Austrian WCD patients

Sponsors

Medical University of Graz
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients, with a prescribed WCD according to guidelines in an austrian center

Design outcomes

Primary

MeasureTime frameDescription
Number of participants treated with WCD-treated ventricular arrhythmiasduring WCD wearing period; average of 1 yearNumber of participants treated with WCD-treated ventricular arrhythmias

Countries

Austria

Contacts

Primary ContactDaniel Scherr, Assoz. Prof.
daniel.scherr@medunigraz.at004331638512544

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026