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Recruiting NCT03409159

Austrian Left Atrial Appendage Closure Registry

Observational Atrial Fibrillation Left Atrial Appendage Closure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: LAAC.
Who it may be relevant to
Registry conditions: Atrial Fibrillation, Left Atrial Appendage Closure. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Austria
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Left atrial appendage (LAA) occlusion (LAAC) has been introduced to treat patients with indication of oral anticoagulation (OAC) for atrial fibrillation (AF) with contraindication to OAC. This registry aims to document all LAAC procedures in Austria.

Interventions

  • Device LAAC
    Left atrial appendage closure

Primary outcome measures

  • Number of participants with successful left atrial appendage closure, as defined by European Society of Cardiology Guidelines [Time frame: 30 days]
Secondary outcome measures (2)
  • Number of participants with death, stroke or bleeding [Time frame: 5 years]
  • Number of participants with procedure-related adverse events [Time frame: 30 days]

Eligibility criteria

Inclusion criteria

  • Patients who received LAAC in Austria

Exclusion criteria

  • Absence of informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Austria · 1 center
  • Medical University of Graz — Graz

Identifiers

NCT: NCT03409159 · 29-355 ex 16/17

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗