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Ablation of Atrial Fibrillation in Heart Failure Patients (CONTRA-HF)

Primary Purpose

Atrial Fibrillation, Severe Heart Failure

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Cryoablation
Sponsored by
Medical University of Silesia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring cryoablation, conventional treatment of heart failure

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years ≤ age ≤ 75 years
  • optimal pharmacotherapy within the last 3 months
  • New York Heart Association (NYHA) II- IV (out-patient) within the last 3 months
  • AF paroxysmal, persistent or persistant long-lasting
  • at least 1 episode of paroxysmal AF with the duration of ≥ 30 s or AF burden ≥ 10% during 1 month up to 1 year since ICD or CRT-D implantation
  • signed informed consent

Exclusion Criteria:

  • age < 18 years or > 75 years
  • permanent AF
  • contraindications to oral anticoagulation or heparin
  • prior AF ablation
  • chronic kidney disease requiring dialysis
  • untreated hypo- or hyperthyroidism
  • breast feeding
  • pregnancy
  • decompensated heart failure within the last 90 days requiring pressor infusion
  • stroke within the last 3 months
  • myocardial infarction within the last 3 months
  • PCI or CABG within the last 3 months
  • active myocarditis
  • artificial valve replacement surgery
  • severe mitral or aortic stenosis
  • coronary artery disease requiring revascularization
  • heart transplant
  • participation in another study
  • comorbidities with expected survival less than 1 year

Sites / Locations

  • Department of Cardiology, Congenital Heart Diseases and Electrotherapy Medical University of Silesia, Silesian Center of Heart DiseasesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Cryoablation

Conventional treatment

Arm Description

The pulmonary vein (PV) isolation in patients randomized to intervention group.

Pharmacological treatment according to 2016 ESC (European Society of Cardiology) guidelines for the diagnosis and treatment of acute and chronic heart failure and to 2016 ESC guidelines for the management of atrial fibrillation developed in collaboration with European Association for Cardio-Thoracic Surgery (EACTS).

Outcomes

Primary Outcome Measures

Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
percentage of patients who required intravenous diuretic or pressor administration
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
percentage of patients who died
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
percentage of patients who required mechanical left ventricle support
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
percentage of patients who had a heart transplant

Secondary Outcome Measures

Percentage of patients who had ischaemic cerebral stroke during 12 months follow up
ischaemic cerebral stroke confirmed in computed tomography

Full Information

First Posted
February 9, 2017
Last Updated
November 4, 2017
Sponsor
Medical University of Silesia
Collaborators
Military Institute od Medicine National Research Institute, Clinical Hospital No. 2 Pomeranian Medical University, Szczecin, Poland, Hospital name Pope John Paul, Zamosc, Poland
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1. Study Identification

Unique Protocol Identification Number
NCT03062241
Brief Title
Ablation of Atrial Fibrillation in Heart Failure Patients
Acronym
CONTRA-HF
Official Title
Cryoablation of Atrial Fibrillation in Patients With Severe Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 23, 2017 (Actual)
Primary Completion Date
July 31, 2018 (Anticipated)
Study Completion Date
July 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Silesia
Collaborators
Military Institute od Medicine National Research Institute, Clinical Hospital No. 2 Pomeranian Medical University, Szczecin, Poland, Hospital name Pope John Paul, Zamosc, Poland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to evaluate the impact of cryoablation of atrial fibrillation in patients with severe chronic heart failure (CHF) on long term outcome of CHF and efficacy (endurance) of the procedure itself. The study hypothesis is that cryoablation in eligible patients with CHF and ICD/CRT (implantable cardioverter defibrillator / cardiac resynchronization therapy) implants reduce the number of recurrent CHF hospitalizations, mortality, need for mechanical support of LV (left ventricle) and heart transplant (primary endpoint) at 1 year observation in comparison to traditional (pharmacological) treatment..
Detailed Description
Atrial fibrillation (AF) is one of the most common arrhythmia worldwide and the risk of AF incidence increases with age. The amount of patients suffered from AF is still underestimated due to insufficient diagnosing silent AF. The incidence of patients with silent, asymptomatic AF might be approx. 80% , particularly in patients with heart failure. The most frequent consequence of undiagnosed AF is not only thromboembolism but also heart failure development and loss of quality of life. The incidence of chronic heart failure (CHF), which is the most frequent consequence of coronary heart disease, still increases and nowadays in patients above 70 years affects approx.10%. What is more, AF which is one of the result of CHF occurred in 30% of those patients. Atrial fibrillation ablation is one of the most established method to treat symptomatic patients and its' efficacy is about 70 - 90 %. Hence, the appropriate and effective treatment of those patients might influence not only on the survival but also the quality of life and functionality of health care system. Among many data about AF in patients with impaired LV (left ventricle) systolic function there is still a lack of randomized, multicenter trials which would compare the influence of AF cryoablation with conventional treatment in patients with LVEF (left ventricle ejection fraction) ≤ 35% (despite optimal pharmacotherapy) on long term survival and efficacy. The deficiency in this field was an inspiration to conduct this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Severe Heart Failure
Keywords
cryoablation, conventional treatment of heart failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a Randomized Controlled Trial (RCT), non-blinded, prospective, multicentre performed in up to 4 cardiology centers in Poland. All patients implanted with a dual-chamber implanted cardioverter-defibrillator (ICD) or cardiac resynchronization therapy defibrillator (CRT-D) with Home Monitoring capabilities and history of paroxysmal, persistent or persistant long-lasting AF will be screened for the study. In patient who fulfill all inclusion and none of the exclusion criteria 1 year after ICD or CRT-D implantation, with exclusion of 1 month directly after implantation, a device check-up and AF burden will be performer and assessed. Randomization will be performed using sealed envelopes and will be conducted in the coordinating center of the study PI in all patients who sign informed consent and met all inclusions and none of the exclusion criteria. The cryoablation of AF will be performed within 1 month from randomization in the invasive treatment group.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
330 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cryoablation
Arm Type
Experimental
Arm Description
The pulmonary vein (PV) isolation in patients randomized to intervention group.
Arm Title
Conventional treatment
Arm Type
No Intervention
Arm Description
Pharmacological treatment according to 2016 ESC (European Society of Cardiology) guidelines for the diagnosis and treatment of acute and chronic heart failure and to 2016 ESC guidelines for the management of atrial fibrillation developed in collaboration with European Association for Cardio-Thoracic Surgery (EACTS).
Intervention Type
Procedure
Intervention Name(s)
Cryoablation
Intervention Description
After left atrial appendage (LAA) thrombus exclusion, the transseptal puncture will be performed and intravenous heparin will be administered to achieve Activated Clotting Time (ACT) ≥300 seconds.The pulmonary vein (PV) isolation will be performed. Optimal cryoballoon positioning will be confirmed by PVs angiography. Pulmonary veins isolation will be confirmed by entrance/exit block using appropriate catheter. During cryoablation of the right PVs, high-output right phrenic nerve stimulation will be performed using a diagnostic catheter placed in the superior vena cava. Whenever decrease/loss of pacing capture will be observed, cryoablation will be immediately terminated.
Primary Outcome Measure Information:
Title
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
Description
percentage of patients who required intravenous diuretic or pressor administration
Time Frame
one year
Title
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
Description
percentage of patients who died
Time Frame
one year
Title
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
Description
percentage of patients who required mechanical left ventricle support
Time Frame
one year
Title
Composite outcome of hospitalization due to heart failure worsening, mortality, use of mechanical left ventricle support and heart transplant.
Description
percentage of patients who had a heart transplant
Time Frame
one year
Secondary Outcome Measure Information:
Title
Percentage of patients who had ischaemic cerebral stroke during 12 months follow up
Description
ischaemic cerebral stroke confirmed in computed tomography
Time Frame
one year
Other Pre-specified Outcome Measures:
Title
Percentage of patients with arrhythmias incidence
Description
the effectiveness of the cryoablation assessed on the device interrogation; atrial fibrillation burden at least 30 seconds
Time Frame
one year
Title
Percentage of patients with arrhythmias incidence
Description
the effectiveness of the cryoablation assessed on the clinical symptoms; the presence of arrhythmias' related symptoms
Time Frame
one year
Title
Quality of life assessment
Description
The Minnesota Living with Heart Failure Questionnaire
Time Frame
one year
Title
Left ventricle ejection fraction assessment
Description
transthoracic echocardiography
Time Frame
one year
Title
Patient capacity assessment
Description
six minute walk test
Time Frame
six months
Title
Oxygen consumption assessment
Description
cardio-pulmonary exercise test
Time Frame
six months
Title
Percentage of patients requiring hospitalization because of arrhythmias' incidence or symptoms (atrial fibrillation/ atrial flutter)
Description
patients who required pharmacological or electrical cardioversion
Time Frame
one year
Title
Percentage of biventricular pacing assessment
Description
the percentage of biventricular pacing assessed on the device interrogation
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years ≤ age ≤ 75 years optimal pharmacotherapy within the last 3 months New York Heart Association (NYHA) II- IV (out-patient) within the last 3 months AF paroxysmal, persistent or persistant long-lasting at least 1 episode of paroxysmal AF with the duration of ≥ 30 s or AF burden ≥ 10% during 1 month up to 1 year since ICD or CRT-D implantation signed informed consent Exclusion Criteria: age < 18 years or > 75 years permanent AF contraindications to oral anticoagulation or heparin prior AF ablation chronic kidney disease requiring dialysis untreated hypo- or hyperthyroidism breast feeding pregnancy decompensated heart failure within the last 90 days requiring pressor infusion stroke within the last 3 months myocardial infarction within the last 3 months PCI or CABG within the last 3 months active myocarditis artificial valve replacement surgery severe mitral or aortic stenosis coronary artery disease requiring revascularization heart transplant participation in another study comorbidities with expected survival less than 1 year
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zbigniew Kalarus, MD, Ph.D.
Phone
0048322713414
Email
karzab@sum.edu.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zbigniew Kalarus, MD, Ph.D.
Organizational Affiliation
Department of Cardiology, Congenital Heart Diseases and Electrotherapy Medical University of Silesia, Silesian Center of Heart Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Cardiology, Congenital Heart Diseases and Electrotherapy Medical University of Silesia, Silesian Center of Heart Diseases
City
Zabrze
ZIP/Postal Code
41-800
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zbigniew Kalarus, MD, Ph.D.
Phone
0048322713414
Email
karzab@sum.edu.pl

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25974193
Citation
Xiong Q, Proietti M, Senoo K, Lip GY. Asymptomatic versus symptomatic atrial fibrillation: A systematic review of age/gender differences and cardiovascular outcomes. Int J Cardiol. 2015 Jul 15;191:172-7. doi: 10.1016/j.ijcard.2015.05.011. Epub 2015 May 7.
Results Reference
background
PubMed Identifier
25890871
Citation
Vaidya K, Arnott C, Russell A, Masson P, Sy RW, Patel S. Pulmonary Vein Isolation Compared to Rate Control in Patients with Atrial Fibrillation: A Systematic Review and Meta-analysis. Heart Lung Circ. 2015 Aug;24(8):744-52. doi: 10.1016/j.hlc.2015.02.025. Epub 2015 Mar 14.
Results Reference
background
PubMed Identifier
25563708
Citation
Lenarczyk R, Jedrzejczyk-Patej E, Szulik M, Mazurek M, Podolecki T, Kowalczyk J, Kowalski O, Sredniawa B, Kalarus Z; Triple-Site Versus Standard Cardiac Resynchronization Trial (TRUST CRT) Investigators. Atrial fibrillation in cardiac resynchronization recipients with and without prior arrhythmic history. How much of arrhythmia is too much? Cardiol J. 2015;22(3):267-75. doi: 10.5603/CJ.a2014.0102. Epub 2015 Jan 7.
Results Reference
background
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
18946063
Citation
Khan MN, Jais P, Cummings J, Di Biase L, Sanders P, Martin DO, Kautzner J, Hao S, Themistoclakis S, Fanelli R, Potenza D, Massaro R, Wazni O, Schweikert R, Saliba W, Wang P, Al-Ahmad A, Beheiry S, Santarelli P, Starling RC, Dello Russo A, Pelargonio G, Brachmann J, Schibgilla V, Bonso A, Casella M, Raviele A, Haissaguerre M, Natale A; PABA-CHF Investigators. Pulmonary-vein isolation for atrial fibrillation in patients with heart failure. N Engl J Med. 2008 Oct 23;359(17):1778-85. doi: 10.1056/NEJMoa0708234.
Results Reference
result
PubMed Identifier
25920033
Citation
Zhao L, Xu K, Jiang W, Zhou L, Wang Y, Zhang X, Wu S, Liu X. Long-term outcomes of catheter ablation of atrial fibrillation in dilated cardiomyopathy. Int J Cardiol. 2015;190:227-32. doi: 10.1016/j.ijcard.2015.04.186. Epub 2015 Apr 23.
Results Reference
result
PubMed Identifier
25534572
Citation
Bunch TJ, May HT, Bair TL, Jacobs V, Crandall BG, Cutler M, Weiss JP, Mallender C, Osborn JS, Anderson JL, Day JD. Five-year outcomes of catheter ablation in patients with atrial fibrillation and left ventricular systolic dysfunction. J Cardiovasc Electrophysiol. 2015 Apr;26(4):363-370. doi: 10.1111/jce.12602. Epub 2015 Feb 11.
Results Reference
result
PubMed Identifier
26217925
Citation
Rillig A, Makimoto H, Wegner J, Lin T, Heeger C, Lemes C, Fink T, Metzner A, Wissner E, Mathew S, Wohlmuth P, Kuck KH, Tilz RR, Ouyang F. Six-Year Clinical Outcomes After Catheter Ablation of Atrial Fibrillation in Patients With Impaired Left Ventricular Function. J Cardiovasc Electrophysiol. 2015 Nov;26(11):1169-1179. doi: 10.1111/jce.12765. Epub 2015 Sep 3.
Results Reference
result
PubMed Identifier
25431023
Citation
Schwartzman D, Housel D, Bazaz R, Jain S, Saba S, Gorcsan J 3rd, Adelstein E. A pilot study to assess benefit of atrial rhythm control after cardiac resynchronization therapy and atrioventricular node ablation. Pacing Clin Electrophysiol. 2015 Feb;38(2):275-81. doi: 10.1111/pace.12535. Epub 2014 Nov 27.
Results Reference
result

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Ablation of Atrial Fibrillation in Heart Failure Patients

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