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Catheter Ablation vs. Standard Conventional Treatment in Patients With LV Dysfunction and AF (CASTLE-AF)

Primary Purpose

Atrial Fibrillation, Heart Failure

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Radiofrequency ablation
Conventional treatment
Sponsored by
Biotronik SE & Co. KG
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Atrial fibrillation, Ablation, Heart failure, Home Monitoring

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

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.

Outcomes

Primary Outcome Measures

All-cause mortality or worsening heart failure requiring unplanned hospitalization

Secondary Outcome Measures

All-cause mortality Cardiovascular mortality Unplanned hospitalization due to cardiovascular reason Worsening heart failure requiring unplanned hospitalization Cerebrovascular accidents Left ventricular function Exercise tolerance Quality of life

Full Information

First Posted
February 22, 2008
Last Updated
May 17, 2017
Sponsor
Biotronik SE & Co. KG
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1. Study Identification

Unique Protocol Identification Number
NCT00643188
Brief Title
Catheter Ablation vs. Standard Conventional Treatment in Patients With LV Dysfunction and AF
Acronym
CASTLE-AF
Official Title
Catheter Ablation Versus Standard Conventional Treatment in Patients With Left Ventricular Dysfunction and Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
January 2008 (Actual)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Biotronik SE & Co. KG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Atrial fibrillation (AF) is the most common arrhythmia encountered in clinical practice. The incidence and prevalence of AF increase exponentially with increasing age and AF is associated with higher mortality, more frequent hospitalization, and lower quality of life. Furthermore, AF is often associated with heart failure. The majority of AF is initiated by ectopic foci found primarily in the pulmonary veins. It was shown that catheter ablation of those veins could eliminate episodes of AF. In patients with heart failure, catheter ablation could improve cardiac function, symptoms and quality of life. It remains still unknown whether AF ablation is more effective than conventional treatment in terms of mortality and morbidity.
Detailed Description
Atrial fibrillation (AF) is the most common arrhythmia encountered in clinical practice; its incidence and prevalence increase exponentially with increasing age and it is associated with increased mortality, more frequent hospitalization, and decreased quality of life. An initial approach to the cure of patients suffering from AF was surgical intervention with the Maze procedure, which involved the creation of linear lesions in the atria to break the re-entrant wavefronts responsible for maintenance of AF. Subsequently, less invasive procedures have been developed to achieve the same results. One of them is catheter based radio frequency ablation, in which a catheter is placed in the heart percutaneously, followed by application of electrical energy to the target regions, thereby creating a permanent lesion. The origin of AF is often localized in the pulmonary veins (PVs); therefore one common approach is to ablate them in order to electrically isolate them from the left atrium (LA). Several strategies have been developed, such as linear, segmental, circumferential, and double-lasso. Additionally, other anatomical regions such as the right atrium (RA), superior vena cava (SVC), and coronary sinus (CS) can be ablated in order to eliminate non-PV drivers of AF. Heart failure (HF) is frequently a chronic and lethal condition, causing substantial morbidity and, after initial diagnosis, results in mortality rates which come close to or exceed those of many malignancies. Both AF and HF have a significant impact on the health care expenditures. The two diseases often coexist, there is a complex interaction between them: many of the processes that predispose to HF, such as hypertension, diabetes, coronary artery disease, and valvular heart disease, are also risk factors for the development of AF. Similarly, many of the echocardiographic findings that are common in patients with HF, including LA enlargement, increased left ventricular (LV) wall thickness, and reduced LV fractional shortening, predispose patients in the development of AF. In small groups of patients suffering from HF and AF, radio frequency ablation has been performed; the restoration of sinus rhythm resulted in the improvement of quality of life, exercise performance, and cardiac parameters like ejection fraction and fractional shortening. It is still unknown if such therapy is also effective in reducing mortality and morbidity. CASTLE-AF is a prospective, unblinded, randomized, multicenter study whose aim is to compare the effect of radio frequency catheter-based ablation on mortality and morbidity with that of conventional treatment in HF subjects with AF. About 420 patients with LV dysfunction (ejection fraction ≤ 35%) and New York Heart Association (NYHA) class ≥ II, already implanted with a dual chamber implantable cardioverter defibrillator (ICD) with Home Monitoring® capabilities, will be enrolled and randomized 1:1 to undergo either AF ablation or standard treatment as indicated in the American College of Cardiology (ACC)/American Heart Association (AHA)/European Society of Cardiology (ESC) 2006 guidelines for the management of patients with AF. In addition to planned and unplanned visits, the ablated patients will be constantly monitored remotely via Home Monitoring®, in order to detect any recurrences of AF episodes, even if non-symptomatic or short in duration, during an observational period of minimum 3 years for each patient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Heart Failure
Keywords
Atrial fibrillation, Ablation, Heart failure, Home Monitoring

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
398 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
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.
Arm Title
2
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency ablation
Intervention Description
Radiofrequency ablation of atrial fibrillation
Intervention Type
Other
Intervention Name(s)
Conventional treatment
Intervention Description
The best medical treatment according to the ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult and the ACC/AHA/ESC 2006 Guidelines for Management of Patients with Atrial Fibrillation.
Primary Outcome Measure Information:
Title
All-cause mortality or worsening heart failure requiring unplanned hospitalization
Time Frame
7 years
Secondary Outcome Measure Information:
Title
All-cause mortality Cardiovascular mortality Unplanned hospitalization due to cardiovascular reason Worsening heart failure requiring unplanned hospitalization Cerebrovascular accidents Left ventricular function Exercise tolerance Quality of life
Time Frame
7 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johannes Brachmann, Prof. Dr.
Organizational Affiliation
Klinikum Coburg, Germany
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nassir F. Marrouche, Dr.
Organizational Affiliation
Division of Cardiology, University of Utah Health Sciences Cente, Salt Lake City, Utah, United States
Official's Role
Study Chair
Facility Information:
Facility Name
Royal Adelaide Hospital
City
Adelaide
Country
Australia
Facility Name
Royal Brisbane and Women's Hospital
City
Herston
Country
Australia
Facility Name
A. ö. Krankenhaus der Elisabethinen Linz
City
Linz
Country
Austria
Facility Name
Allgemeines Krankenhaus der Stadt Wien
City
Wien
Country
Austria
Facility Name
Herz- und Diabeteszentrum Nordrhein-Westfalen
City
Bad Oeynhausen
Country
Germany
Facility Name
Charité Campus Mitte
City
Berlin
Country
Germany
Facility Name
Charité Campus Virchow-Klinikum
City
Berlin
Country
Germany
Facility Name
Franz-Volhard-Klinik, Universitätsklinikum Charité
City
Berlin
Country
Germany
Facility Name
Vivantes-Klinikum am Urban
City
Berlin
Country
Germany
Facility Name
Städtische Kliniken Bielefeld
City
Bielefeld
Country
Germany
Facility Name
St. Marien Hospital
City
Bonn
Country
Germany
Facility Name
Zentralkrankenhaus Links der Weser, Siebels & Langes Partnerschaft
City
Bremen
Country
Germany
Facility Name
Klinikum Coburg
City
Coburg
Country
Germany
Facility Name
Evangelisches Krankenhaus Düsseldorf
City
Düsseldorf
Country
Germany
Facility Name
Kardiocentrum Frankfurt an der Klinik Rotes Kreuz
City
Frankfurt am Main
Country
Germany
Facility Name
Universitätsklinikum der Ernst-Moritz-Arndt-Universität Greifswald
City
Greifswald
Country
Germany
Facility Name
Krankenhaus Landshut-Achdorf
City
Landshut
Country
Germany
Facility Name
Klinikum Lüdenscheid
City
Lüdenscheid
Country
Germany
Facility Name
Deutsches Herzzentrum München
City
München
Country
Germany
Facility Name
St. Vincenz-Krankenhaus
City
Paderborn
Country
Germany
Facility Name
Universitätsklinikum Rostock
City
Rostock
Country
Germany
Facility Name
Semmelweis Medical University
City
Budapest
Country
Hungary
Facility Name
The Debrecen University of Medicine
City
Debrecen
Country
Hungary
Facility Name
Antonius Ziekenhuis
City
Nieuwegein
Country
Netherlands
Facility Name
Erasmus Medical Center
City
Rotterdam
Country
Netherlands
Facility Name
Isala Klinieken
City
Zwolle
Country
Netherlands
Facility Name
National Institute of Cardiology
City
Warszawa
Country
Poland
Facility Name
HRD Surgical Department; Federal Centre of Cardiovascular Surgery
City
Krasnoyarsk
Country
Russian Federation
Facility Name
N.S.B.R.I. of Circulation Pathology
City
Novosibirsk
Country
Russian Federation
Facility Name
Arrhythmology Department; Federal Heart Blood and Endocrinology Center n.a. V. A. Almazov
City
Saint Petersburg
Country
Russian Federation
Facility Name
FSBI Research Institute of Cardiology, Siberian Branch of RAMS
City
Tomsk
Country
Russian Federation
Facility Name
The Heart Hospital
City
London
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
It is planned to publish results of this investigation in peer-reviewed journals (online: open-access), but it is not yet decided to annex individual participant data (IPD).
Citations:
PubMed Identifier
19659616
Citation
Marrouche NF, Brachmann J; CASTLE-AF Steering Committee. Catheter ablation versus standard conventional treatment in patients with left ventricular dysfunction and atrial fibrillation (CASTLE-AF) - study design. Pacing Clin Electrophysiol. 2009 Aug;32(8):987-94. doi: 10.1111/j.1540-8159.2009.02428.x.
Results Reference
background
PubMed Identifier
33640355
Citation
Brachmann J, Sohns C, Andresen D, Siebels J, Sehner S, Boersma L, Merkely B, Pokushalov E, Sanders P, Schunkert H, Bansch D, Dagher L, Zhao Y, Mahnkopf C, Wegscheider K, Marrouche NF. Atrial Fibrillation Burden and Clinical Outcomes in Heart Failure: The CASTLE-AF Trial. JACC Clin Electrophysiol. 2021 May;7(5):594-603. doi: 10.1016/j.jacep.2020.11.021. Epub 2021 Feb 24.
Results Reference
derived
PubMed Identifier
29385358
Citation
Marrouche NF, Brachmann J, Andresen D, Siebels J, Boersma L, Jordaens L, Merkely B, Pokushalov E, Sanders P, Proff J, Schunkert H, Christ H, Vogt J, Bansch D; CASTLE-AF Investigators. Catheter Ablation for Atrial Fibrillation with Heart Failure. N Engl J Med. 2018 Feb 1;378(5):417-427. doi: 10.1056/NEJMoa1707855.
Results Reference
derived
Links:
URL
http://www.castle-af.org
Description
Click here for more information about this study: CASTLE-AF

Learn more about this trial

Catheter Ablation vs. Standard Conventional Treatment in Patients With LV Dysfunction and AF

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