Partnerstudie – CABA-HFPEF

CAtheter-Based ablation of Atrial fibrillation vs. conventional treatment in patients with Heart Failure with Preserved Ejection Fraction (CABA-HFPEF)

Sponsor´s Protocol Code: CABA-HFPEF-DZHK27

ClinicalTrials.gov Identifier: NCT05508256

Investigator-initiated multicentre study with prospective parallel group comparison with randomised, open group allocation and blinded endpoint analysis (so-called PROBE design)

The aim of the study is to investigate whether catheter ablation of atrial fibrillation (AF) can prevent serious cardiovascular events in patients with heart failure with preserved or mildly reduced ejection fraction (HFpEF or HFmrEF).

Atrial fibrillation is an irregular heart rhythm in which the upper chambers of the heart (atria) beat very quickly. Atrial fibrillation can increase the risk of blood clots forming in the heart. These can break loose and travel to the brain, where they can trigger a stroke. Catheter ablation is a procedure that restores the normal heart rhythm. However, even patients who successfully undergo this treatment may have an increased risk of stroke compared to people who have never had atrial fibrillation.

To reduce the risk of stroke, patients are prescribed one of two drugs after catheter ablation: a drug that inhibits the function of blood platelets (acetylsalicylic acid (ASA), e.g. Aspirin®) or a blood thinner (also known as an anticoagulant, e.g. rivaroxaban).The aim of this study is to find out which of these two types of treatment is best at preventing strokes.

Principal Investigator

Klinik für Kardiologie, Angiologie und Intensivmedizin
Deutsches Herzzentrum der Charité Berlin

Regulatory EC submissions in Germany and Austria, committee support, ISF preparation, review of study documents, organisation of investigator meetings, social media