saxOnian RegIstry analyzinG and followINg left atrial Appendage cLosure

saxOnian RegIstry analyzinG and followINg left atrial Appendage cLosure - ORIGINAL

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00023803

Enrollment

1000

Registered

2020-12-15

Start date

2014-07-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

I48 I63

Interventions

Group 1: Planned examinations as part of the study: TTE and TEE 6 weeks, 6 months, 1, 2, 3, 4 and 5 years after the intervention

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Presence of non-valvular paroxysmal, persistent or permanent atrial fibrillation Age over 18 years Written consent

Exclusion criteria

Exclusion criteria: Malignant tumor disease with life expectancy <12 months Pregnancy Patients who are unable to give the written consent

Design outcomes

Primary

Measure	Time frame
The aim of this register is, on the one hand, to analyze the safety and effectiveness of the procedure in patients with a high risk of bleeding in everyday clinical practice and, on the other hand, to evaluate hemorrhagic and thromboembolic events over the long term.	—

Secondary

Measure	Time frame
To evaluate hemorrhagic and thromboembolic events in long term follow up	—

Countries

Germany

Contacts

Public ContactLucie Kretzler

Berlin Institute of Health (BIH)

lucie.kretzler@charite.de030 450 643584

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 12, 2026