LAAC-registry: Clinical Outcome After Echocardiography-guided LAA-closure
Recruiting · NCT04628078 · Observational (researchers observe without assigning treatment) · Lead sponsor: Insel Gruppe AG, University Hospital Bern
View the official record on ClinicalTrials.gov →Interventions studied
Use of echocardiography guidance for LAAC
What this trial is about
The study aims at comparing, in a large cohort of consecutive clinically indicated left atrial appendage closure, clinical and imaging outcomes between different subpopulations.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- 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
Exclusion criteria
- 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.
Where it is running
1 location listed.
- Bern University Hospital Inselspital - Bern, Switzerland