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Catheter Ablation Versus Standard Conventional Treatment in Heart Failure Patients With Atrial Fibrillation (CASTLE-AF)
This study is currently recruiting participants.
Verified by Biotronik GmbH & Co. KG, June 2008
Sponsored by: Biotronik GmbH & Co. KG
Information provided by: Biotronik GmbH & Co. KG
ClinicalTrials.gov Identifier: NCT00643188
  Purpose

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 qualitiy of life. It remains still unknown wether AF ablation is more effective than conventional treatment in termns of mortality and morbidity.


Condition Intervention Phase
Atrial Fibrillation
Heart Failure
Procedure: Radiofrequency ablation
Other: Conventional treatment
Phase IV

Genetics Home Reference related topics: Brugada syndrome familial atrial fibrillation short QT syndrome
MedlinePlus related topics: Heart Failure
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Parallel Assignment, Efficacy Study
Official Title: Catheter Ablation Versus Standard Conventional Treatment in Patients With Left Ventricular Dysfunction and Atrial Fibrillation

Further study details as provided by Biotronik GmbH & Co. KG:

Primary Outcome Measures:
  • All-cause mortality or worsening heart failure requiring unplanned hospitalization [ Time Frame: 5 years ] [ Designated as safety issue: No ]

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 [ Time Frame: 5 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 420
Study Start Date: January 2008
Estimated Study Completion Date: January 2013
Estimated Primary Completion Date: January 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Radiofrequency ablation of atrial fibrillation
Procedure: Radiofrequency ablation
Radiofrequency ablation of atrial fibrillation
2: Active Comparator
Conventional treatment according to the respective current guidelines
Other: Conventional treatment
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.

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 radiofrequency 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, radiofrequency 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, multi-center study whose aim is to compare the effect of radiofrequency 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 ACC/AHA/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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Symptomatic paroxysmal or persistent atrial fibrillation
  • Failure or intolerance of Amiodarone or unwillingness to take Amiodarone
  • LVEF <= 35%
  • NYHA >= II
  • Indication for ICD therapy due to primary prevention
  • Dual chamber ICD with Home Monitoring capabilities already implanted
  • Patient is willing and able to comply with the protocol and has written informed consent
  • Sufficiant GPRS network coverage in the patient`s area
  • 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
  • Indication for Cardiac Resynchronization Therapy
  • 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 HTX
  • 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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00643188

Contacts
Contact: Kuno Muench +49-9131-8924-7827 kuno.muench@biotronik.com
Contact: Jochen Proff +49-9131-8924-7810 jochen.proff@biotronik.com

  Show 34 Study Locations
Sponsors and Collaborators
Biotronik GmbH & Co. KG
Investigators
Study Chair: Johannes Brachmann, Prof. Dr. Klinikum Coburg, Germany
Study Chair: Nassir F. Marrouche, Dr. Division of Cardiology, University of Utah Health Sciences Cente, Salt Lake City, Utah, United States
  More Information

Responsible Party: Klinikum Coburg, Germany ( Professor Dr. Johannes Brachmann )
Study ID Numbers: EP020
Study First Received: February 22, 2008
Last Updated: June 6, 2008
ClinicalTrials.gov Identifier: NCT00643188  
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Keywords provided by Biotronik GmbH & Co. KG:
Atrial fibrillation
Ablation
Heart failure
Home Monitoring

Study placed in the following topic categories:
Ventricular Dysfunction
Heart Failure
Heart Diseases
Ventricular Dysfunction, Left
Atrial Fibrillation
Arrhythmias, Cardiac

Additional relevant MeSH terms:
Pathologic Processes
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009