Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrillation Patients (CAAN-AF)

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2014 by University of Adelaide
Sponsor:
Collaborators:
Medtronic
St. Jude Medical
Boston Scientific Corporation
Information provided by (Responsible Party):
Prashanthan Sanders, University of Adelaide
ClinicalTrials.gov Identifier:
NCT01522898
First received: January 25, 2012
Last updated: June 24, 2014
Last verified: June 2014
  Purpose

Cardiac resynchronization therapy (CRT) is a treatment for heart failure in patients who also suffer from ventricular dyssynchrony, a form of uncoordinated contraction of the ventricle (lower pumping chamber of the heart). In the past decade, CRT has become an established treatment for heart failure patients who are in normal rhythm, called sinus rhythm. An important subset of heart failure patients are those with atrial fibrillation (AF), who make up around 1 in 4 HF patients, and are over-represented amongst HF patients with more advanced symptoms. In heart failure patients with AF, CRT has proven not to be as effective as in sinus rhythm, due to competition between beats generated by the CRT device and beats conducted from the heart's own electrical conduction system. In the current study, we aim to test the hypothesis that ablating the AV node, which controls electrical conduction from the heart's atria (top chamber) to its ventricles (lower chambers), will improve survival and heart failure symptoms in CRT patients with co-existent AF. The results are important, because they will provide a way of passing on the benefits of CRT, such as improved survival, less heart failure symptoms, and better quality of life, to heart failure patients who also suffer from AF.


Condition Intervention
Heart Failure
Atrial Fibrillation
Procedure: AV nodal ablation
Drug: Medical Ventricular Rate Control

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Cardiac Resynchronisation Therapy and AV Nodal Ablation Trial in Atrial Fibrillation

Resource links provided by NLM:


Further study details as provided by University of Adelaide:

Primary Outcome Measures:
  • All-cause mortality and non-fatal heart failure events [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: Yes ]

    This is a composite of all-cause mortality and non-fatal heart failure events. All-cause mortality will be determined by a designated clinical events committee.

    Heart Failure events will be documented by clinical data from the hospital In CAAN-AF, a subject will be described as having a "Heart Failure Event" when the subject has symptoms and/or signs consistent with congestive heart failure and:

    • responsive to parenteral diuretic or inotropic support as an outpatient
    • responsive to oral or parenteral diuretic or inotropic support during an inpatient stay


Secondary Outcome Measures:
  • All-cause mortality [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up)f recruitment ] [ Designated as safety issue: Yes ]
    All-cause mortality will be determined after adjudication committee review of clinical records, and death certificate data.

  • Cardiovascular mortality [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: Yes ]
    Cardiovascular deaths will be classified in terms of suddenness and arrhythmic mechanism according to the Hinkle-Thaler criteria.

  • Non-Fatal Heart Failure Events [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]

    Heart Failure events will be documented by clinical data from the hospital In CAAN-AF, a subject will be described as having a "Heart Failure Event" when the subject has symptoms and/or signs consistent with congestive heart failure and:

    • responsive to parenteral diuretic or inotropic support as an outpatient
    • responsive to oral or parenteral diuretic or inotropic support during an inpatient stay

  • 6-minute walking distance [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]
    6-minute walking distance will be measured according to standard criteria.

  • Quality of Life [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]
    Quality of life as assessed by the Short Form 36 (SF-36) questionnaire and Minnesota Living with Heart Failure Questionnaire

  • Unplanned Hospitalization [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: Yes ]
    Unplanned hospital admissions will be assessed by a combination of patient self-report, hospital record and/or treating physician interrogation. The reason, date and duration of hospitalization will be recorded Planned hospitalizations (hospital visits for elective or planned medical interventions) will excluded from this outcome

  • Ventricular arrhythmias requiring device therapy [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]
    Ventricular arrhythmias requiring device therapy will be determined by implantable Cardioverter Defibrillator (ICD) interrogation records and clinical records. At each site, the number, duration and type (VT/VF) of device recorded arrhythmias will be recorded, as well as the need for device therapy (anti-tachycardia pacing and/or ICD shocks).


Other Outcome Measures:
  • Inappropriate shocks [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: Yes ]
    The clinical events committee will review clinical records to ascertain if device therapies are appropriate or inappropriate.

  • Cardiovascular MRI prediction of response [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]
    Cardiovascular MRI will be performed in subjects eligible for this procedure prior to implantation of CRT device, when available. Cardiovascular MRI data will be evaluated for the ability to predict clinical CRT response.

  • Depression [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]
    Depression will be evaluated in all patients at specified clinical follow-up visits with the Center for Epidemiologic Studies Depression Scale (CES-D questionnaire).

  • Ventricular reverse remodelling [ Time Frame: Final-analysis at completion of recruitment and follow-up period (minimum 2 year follow-up) ] [ Designated as safety issue: No ]
    Left ventricular reverse remodeling will be assessed by echocardiographic parameters including left ventricular end systolic volume, left ventricular ejection fraction. An echocardiography core laboratory has been established to process images from individual trial sites for this purpose.


Estimated Enrollment: 590
Study Start Date: March 2013
Estimated Study Completion Date: July 2016
Estimated Primary Completion Date: July 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Medical Rate Control
Medical Rate Control aimed at ventricular rate target of 90 beats per minute. Specific medical therapy to be determined for each patient by individual clinician.
Drug: Medical Ventricular Rate Control
Ventricular Rate Control with target ventricular rate of 90 beats per minute.
Experimental: AV nodal ablation
AV node ablation performed by percutaneous catheter ablation, with endpoint of complete heart block.
Procedure: AV nodal ablation
Percutaneous catheter ablation of the AV node.
Other Name: His Bundle Ablation, AV junctional ablation

  Hide Detailed Description

Detailed Description:

Background: Cardiac Resynchronization Therapy (CRT) is an established treatment in heart failure (HF) patients with ventricular dyssynchrony who remain in sinus rhythm. Available clinical data has shown inferior outcomes of CRT in HF patients with co-existent atrial fibrillation (AF), who comprise up to 27% of HF patients, and are over-represented in advanced HF classes. We hypothesize, based on the results of a systematic review we recently published in the Journal of the American College of Cardiology, that AV nodal ablation may improve survival, heart failure and functional outcomes in CRT recipients with co-existent AF.

Design: This study will be a multicentre, prospective, randomized controlled trial. Patients with ischemic or nonischemic cardiomyopathy heart failure (NYHA II, III or ambulatory class IV), left ventricular dysfunction (EF ≤ 35%), prolonged intraventricular conduction (QRS duration ≥ 120ms), and persistent or permanent AF will be considered for the study. Persistent AF will be defined as patients where obtaining and maintaining sinus rhythm is deemed either not worthwhile, or to be ineffective in the long term, or where both the patient and the physician accept the presence of AF, where rhythm control intervention is, by definition, no longer pursued. Permanent AF is defined as AF where sinus rhythm cannot be restored.

Eligible subjects will be randomized into one of two arms: (1) CRT-D plus AV nodal ablation ("AV nodal ablation arm [AVNA]") or (2) CRT-D alone ("rate control arm").

Enrollment: 590 subjects, with 295 subjects in the AV node ablation arm and 295 subjects in the control arm, will be enrolled. Study patients will undergo stratified randomization at ≥ 30 days after CRT implant. Participants in will sign informed consent and be screened prior to randomisation. After CRT implant, patients will have at least 30 days for optimisation of heart failure therapy, prior to randomisation.

Randomisation: A computer-generated web-based randomisation schedule will be used. Randomisation will be stratified by trial centre. Randomisation is considered the trial entry point.

Outcomes: The primary endpoint is a composite of all cause mortality and non-fatal heart failure events. Secondary endpoints include all-cause mortality, cardiovascular mortality (including classification in terms of suddenness and arrhythmic mechanism by prespecified Hinkle-Thaler criteria), non-fatal heart failure events, 6-minute walking test distance, quality of life, unplanned hospitalization, and ventricular arrhythmias requiring device therapy, inappropriate shocks, cardiovascular MRI prediction of response, percentage pacing and prediction of response to therapy, ventricular reverse remodeling.

Statistical Plan: The study is powered to find a 25% relative reduction in event rate, with sample sizes calculated assuming a two-tailed α=0.05,1-β=0.80, and 10% sample size increment allow for to drop in the event rate (AV nodal ablation arm), drop out or cross-over (feasibly, control to AVNA arm only). It is planned to perform three interim (0.25, 0.5 0.75 information fractions) and a final analysis requiring 295 patients per arm with a final P-value at ≤ 0.045; stopping rules according to the method of O'Brien and Fleming. The boundaries (z scores: ±4.332, ±2.963, ±2.359, ±2.014; and nominal P-values: 0.000015, 0.0031, 0.014, 0.044)) were derived using the statistical package PASS (V12). Outside of these defined analyses, the Data Safety Monitoring Board (DSMB) will have access to data reports and will be able to stop the trial at any time.

All analyses will be based on the intention-to-treat principle. The primary (binary) mortality-outcome will be analysed using the Cochran-Mantel-Haenszel statistic and logistic regression with pre-specified (baseline) covariates. Time-to-event analyses will be initially undertaken by the Kaplan-Meier survival analysis approach. Key secondary outcomes such as all-cause mortality, cardiovascular mortality, unplanned hospitalisation, and rates of ventricular arrhythmia episodes will be analysed using either Cox proportional hazards models or Fine and Gray competing risks regression as appropriate. Continuous secondary outcomes such as the 6-minute walking distance, Short Form 36 (SF36) scores, Minnesota Living with Heart Failure (MLWHF) score will be compared between randomised groups over time using linear mixed effects models.

Significance and Impact: The study will answer a central clinical question directly impacting the care of HF patients with AF, and will be expected to change current HF management guidelines.

  Eligibility

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

Inclusion Criteria:

  • Age ≥ 18 years old
  • Persistent (≥ 1 month) or permanent atrial fibrillation. Persistent AF will be where obtaining and maintaining sinus rhythm is deemed either not worthwhile, or to be ineffective in the long term, or where both the patient and physician accept the presence of AF, where rhythm control intervention is, by definition no longer pursued. Permanent AF is defined as atrial fibrillation where sinus rhythm cannot be restored.
  • NYHA class II , III or ambulatory class IV heart failure
  • Left Ventricular Ejection Fraction (LVEF) ≤ 35% by objective criteria such as echocardiography, or cardiac MRI
  • QRS duration on 12-lead ECG ≥ 120ms
  • Able and willing to comply with all pre-, post- and follow-up testing and requirements.

Exclusion Criteria:

  • age < 18 years
  • pregnancy
  • previous AV nodal ablation
  • Second or third degree AV block
  • Inability to provide informed consent
  • life expectancy less than 24 months due to co-morbid illness other than heart failure erg cancer, end-stage renal disease, liver failure
  • Paroxysmal Atrial Fibrillation that self terminates within 7 days
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01522898

Contacts
Contact: Prashanthan Sanders, MBBS PhD +61-8-8222-2723 prash.sanders@adelaide.edu.au
Contact: Anand N Ganesan, MBBS PhD +61-8-8222-2723 anand.ganesan@adelaide.edu.au

Locations
Australia, Australian Capital Territory
Canberra Hospital Recruiting
Canberra, Australian Capital Territory, Australia, 2605
Contact: Walter Abhayaratna, MBBS    02 6244 2445      
Principal Investigator: Walter Abhayaratna, MBBS         
Australia, New South Wales
Concord Hospital Recruiting
Concord, New South Wales, Australia
Contact: Jun Wu    0296765264      
Principal Investigator: Ray Sy, MBBS PhD         
Sub-Investigator: Maros Elsik, MBBS PhD         
John Hunter Hospital Recruiting
New Lambton, New South Wales, Australia, 2305
Contact: Anne Gordon, MD    (02) 4921 4720      
Principal Investigator: Malcolm Barlow, MD         
Sub-Investigator: Bradley Wilsmore, MBBS         
Sub-Investigator: James Leitch, MBBS         
Royal Prince Alfred Hospital Recruiting
Sydney, New South Wales, Australia
Principal Investigator: Raymond Sy, MBBS PhD         
Australia, Queensland
Royal Brisbane Hospital Recruiting
Brisbane, Queensland, Australia
Contact: Leeanne Palethorpe    0736365281      
Principal Investigator: Karin Chia, MBBS PhD         
Prince Charles Hospital Recruiting
Chermside, Queensland, Australia, 4032
Contact: Bernice Enever    (07) 3139 5906      
Principal Investigator: Haris Haqqani, MBBS PhD         
Princess Alexandra Hospital Recruiting
Wollongabba, Queensland, Australia
Contact: Cindy Hall    0731765145      
Contact: Charmain Seig         
Principal Investigator: Gerald Kaye, MBBS         
Australia, South Australia
Royal Adelaide Hospital Recruiting
Adelaide, South Australia, Australia, 5000
Contact: Vanessa Maxwell    +61-8-8222-2723    vanessa.maxwell@adelaide.edu.au   
Principal Investigator: Prashanthan Sanders, MBBS PhD         
Sub-Investigator: Anand N Ganesan, MBBS PhD         
Sub-Investigator: Glenn D Young, MBBS         
Sub-Investigator: Kurt C Roberts-Thomson, MBBS PhD         
Sub-Investigator: Dennis H Lau, MBBS PhD         
Sub-Investigator: Richard Hillock, MBBS         
Flinders Medical Centre Recruiting
Bedford Park, South Australia, Australia, 5042
Contact: Deirdre Murphy    08-8820 4440      
Principal Investigator: Andrew McGavigan, MBChB, MD         
Sub-Investigator: William Heddle, MBBS         
Sub-Investigator: Cameron Singleton, MBBS PhD         
Australia, Victoria
Monash Medical Centre Recruiting
Clayton, Victoria, Australia, 3168
Contact: Mauro Baldi         
Principal Investigator: Jeff Allison         
Sub-Investigator: Khang Looi         
Northern Hospital Recruiting
Epping, Victoria, Australia
Contact: Rita Wong         
Principal Investigator: Uwais Mohamed         
Geelong Hospital Recruiting
Geelong, Victoria, Australia, 3220
Contact: Mark Perrin, MBBS    03 4215 1955      
Principal Investigator: Mark Perrin, MBBS         
Austin Hospital Recruiting
Heidelburg, Victoria, Australia, 3084
Contact: Andrew Tinney         
Principal Investigator: David O'Donnell, MBBS PhD         
The Alfred Hospital Recruiting
Melbourne, Victoria, Australia
Contact: Peter Kistler, MBBS PhD         
Melbourne Private Hospital Recruiting
Melbourne, Victoria, Australia
Contact: Juliet Ward         
Principal Investigator: Jonathan Kalman, MBBS PhD         
Royal Melbourne Hospital Recruiting
Parkville, Victoria, Australia, 3050
Contact: Karen L Halloran    +61393495400    Karen.Halloran@mh.org.au   
Principal Investigator: Jonathan M Kalman, MBBS PhD         
Australia, Western Australia
Royal Perth Hospital Recruiting
Perth, Western Australia, Australia
Contact: Mary Vorster    (08) 9224 8069      
Contact: Michelle Bonner         
Principal Investigator: Vince Paul, MBBS PhD         
Sub-Investigator: Timothy Gattorna, MBBS         
Sir Charles Gairdner Hospital Recruiting
Perth, Western Australia, Australia, 6009
Contact: Paul Stobie, MBBS    08 9346 4534      
Principal Investigator: Paul Stobie, MBBS         
New Zealand
Tauranga Hospital Recruiting
Tauranga, Bay of Plenty, New Zealand, 3143
Contact: Dean Boddington, MBBS    07 579 8000      
Principal Investigator: Dean Boddington         
Auckland City Hospital Recruiting
Auckland, New Zealand, 1142
Contact: Nigel Lever       nlever@adhb.gov.nz   
Principal Investigator: Nigel Lever         
Waikato Hospital Recruiting
Hamilton, New Zealand, 3240
Contact: Liz Low    7839 7136      
Principal Investigator: Martin Stiles, MBChB PhD         
Wellington Hospital Recruiting
Wellington, New Zealand, 6021
Contact: Alejandro Jimenez       alejandro.jimenez@ccdhb.org.nz   
Principal Investigator: Alejandro Jimenez         
Sponsors and Collaborators
University of Adelaide
Medtronic
St. Jude Medical
Boston Scientific Corporation
Investigators
Principal Investigator: Prashanthan Sanders, MBBS PhD University of Adelaide
  More Information

No publications provided

Responsible Party: Prashanthan Sanders, Director, Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital, University of Adelaide
ClinicalTrials.gov Identifier: NCT01522898     History of Changes
Other Study ID Numbers: RAH-HREC-Protocol-#111234
Study First Received: January 25, 2012
Last Updated: June 24, 2014
Health Authority: Australia: Department of Health and Ageing Therapeutic Goods Administration
Australia: Human Research Ethics Committee
Australia: National Health and Medical Research Council

Keywords provided by University of Adelaide:
Heart Failure
Atrial Fibrillation

Additional relevant MeSH terms:
Atrial Fibrillation
Heart Failure
Arrhythmias, Cardiac
Heart Diseases
Cardiovascular Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on July 28, 2014