- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02816047
Austrian Wearable Cardioverter Defibrillator Registry
Indications for and Experience With the Wearable Cardioverter Defibrillator (WCD) - Austrian WCD Registry
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Daniel Scherr, Assoz. Prof.
- Phone Number: 004331638512544
- Email: daniel.scherr@medunigraz.at
Study Locations
-
-
-
Graz, Austria, 8036
- Recruiting
- Medical University of Graz/ Division of Cardiology
-
Contact:
- Tanja Odeneg, MSc
- Phone Number: 004331638530199
- Email: tanja.odeneg@medunigraz.at
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients, with a prescribed WCD according to guidelines in an austrian center
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of participants treated with WCD-treated ventricular arrhythmias
Time Frame: during WCD wearing period; average of 1 year
|
Number of participants treated with WCD-treated ventricular arrhythmias
|
during WCD wearing period; average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Daniel Scherr, Assoz. Prof., Medical University of Graz/ Division of Cardiology
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KardioScherr1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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