LAAC-registry: Clinical Outcome After Echocardiography-guided LAA-closure
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInsel Gruppe AG, University Hospital Bern
About this trial
The study aims at comparing, in a large cohort of consecutive clinically indicated left atrial appendage closure, clinical and imaging outcomes between different subpopulations.
Eligibility criteria
Qualifiers
Age> 18
Written informed consent to participate in the study
Patients with paroxysmal, persistent, or permanent non-valvular AF and CHA2DS2-VASc Score of ≥2 that are planned for an elective LAA-closure
Anatomic characteristics allow placement of a CE marked device, dedicated for LAAC
Disqualifiers
None. Considering the nature of the project, which is to prospectively collect information on all patients treated with LAAC in our center, we will only exclude patients unwilling to sign the informed consent.
Trial design
Treatments tested in this trial
- Use of echocardiography guidance for LAAC
Treatment groups
No treatment groups listed
Locations
1Bern University Hospital Inselspital3010, Bern Switzerland
Sponsors and collaborators
Insel Gruppe AG, University Hospital Bern
Lead sponsor
Source ClinicalTrials.gov