Catheter Ablation vs. Standard Conventional Treatment in Patients With LV Dysfunction and AF (CASTLE-AF)
Atrial Fibrillation, Heart Failure
About this trial
This is an interventional treatment trial for Atrial Fibrillation focused on measuring Atrial fibrillation, Ablation, Heart failure, Home Monitoring
Eligibility Criteria
Inclusion Criteria:
- Symptomatic paroxysmal or persistent atrial fibrillation
- Failure or intolerance of antiarrhythmic drug therapy or unwillingness to take antiarrhythmic drugs
- Left Ventricular Ejection Fraction <= 35%
- NYHA >= II
- ICD for primary or secondary prevention with atrial sensing capabilities or Cardiac Resynchronization Therapy plus Defibrillator (CRT-D) device, both with Home Monitoring® technology already implanted
- Patient is willing and able to comply with the protocol and has written informed consent
- Age >= 18 years
Exclusion Criteria:
- Contraindication for chronic anticoagulation therapy and heparin
- Documented left atrial diameter > 6 cm
- Previous left heart ablation procedure for atrial fibrillation
- Acute coronary syndrome, cardiac surgery, angioplasty or stroke within 2 months prior to enrollment
- Untreated hypothyroidism or hyperthyroidism
- Enrollment in another investigational drug or device study
- Woman currently pregnant or breastfeeding or not using reliable contraceptive measures during fertility age
- Mental or physical inability to take part in the study
- Listed for heart transplant
- Cardiac assist device implanted
- Planned cardiovascular intervention
- Life expectancy ≤ 12 months
- Uncontrolled hypertension
- Requirement for dialysis due to terminal renal failure
- Participation in another telemonitoring concept
Sites / Locations
- Royal Adelaide Hospital
- Royal Brisbane and Women's Hospital
- A. ö. Krankenhaus der Elisabethinen Linz
- Allgemeines Krankenhaus der Stadt Wien
- Herz- und Diabeteszentrum Nordrhein-Westfalen
- Charité Campus Mitte
- Charité Campus Virchow-Klinikum
- Franz-Volhard-Klinik, Universitätsklinikum Charité
- Vivantes-Klinikum am Urban
- Städtische Kliniken Bielefeld
- St. Marien Hospital
- Zentralkrankenhaus Links der Weser, Siebels & Langes Partnerschaft
- Klinikum Coburg
- Evangelisches Krankenhaus Düsseldorf
- Kardiocentrum Frankfurt an der Klinik Rotes Kreuz
- Universitätsklinikum der Ernst-Moritz-Arndt-Universität Greifswald
- Krankenhaus Landshut-Achdorf
- Klinikum Lüdenscheid
- Deutsches Herzzentrum München
- St. Vincenz-Krankenhaus
- Universitätsklinikum Rostock
- Semmelweis Medical University
- The Debrecen University of Medicine
- Antonius Ziekenhuis
- Erasmus Medical Center
- Isala Klinieken
- National Institute of Cardiology
- HRD Surgical Department; Federal Centre of Cardiovascular Surgery
- N.S.B.R.I. of Circulation Pathology
- Arrhythmology Department; Federal Heart Blood and Endocrinology Center n.a. V. A. Almazov
- FSBI Research Institute of Cardiology, Siberian Branch of RAMS
- The Heart Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
1
2
Radiofrequency ablation of atrial fibrillation: Subjects assigned to the catheter AF ablation strategy will undergo ablation within 48 hours after baseline evaluation. The aim of the procedure is to achieve isolation of all Pulmonary Veins (PVs) and to restore sinus rhythm. Only radiofrequency catheter based AF ablation is permitted; other methods, like cryoablation, ultrasound and laser, are not permitted in this study. Before ablation, a transesophageal echocardiogram must be performed in order to rule out presence of atrial thrombi. Anticoagulation should be initiated, or continued, for at least six months post ablation. Six months after successful ablation and in absence of any recurrence of AF, antiarrhythmic drugs should be discontinued.
Conventional treatment: Subjects assigned to the conventional treatment strategy will be treated according to current guidelines for the management of patients with chronic heart failure and/or atrial fibrillation. Efforts to maintain sinus rhythm in this study arm are recommended. Anticoagulation will be initiated, if not already started, and maintained throughout the study according to current guidelines.