Rhythm Control - Catheter Ablation With or Without Anti-arrhythmic Drug Control of Maintaining Sinus Rhythm Versus Rate Control With Medical Therapy and/or Atrio-ventricular Junction Ablation and Pacemaker Treatment for Atrial Fibrillation (RAFT-AF)
A Randomized Ablation-based Atrial Fibrillation Rhythm Control Versus Rate Control Trial in Patients With Heart Failure and High Burden Atrial Fibrillation
Atrial fibrillation and heart failure are two common heart conditions that are associated with an increase in death and suffering. When both of these two conditions occur in a patient the patient's prognosis is poor. These patients have poor life quality and are frequently admitted to the hospital. The treatment of atrial fibrillation in heart failure patients is extremely challenging. Two options for managing the atrial fibrillation are permitting the atrial fibrillation to continue but controlling the heart rate, or to convert the atrial fibrillation rhythm back to normal and try to maintain the heart in sinus rhythm. Until now, the method to keep the patient in normal sinus rhythm is with antiarrhythmic drugs. Studies using antiarrhythmic drugs to control the rhythm failed to show any survival benefit when compared with permitting the patient to be in atrial fibrillation. In the last few years, new development in techniques and technologies now enable catheter ablation (cauterization of tissue in the heart with a catheter) to be a successful treatment in abolishing atrial fibrillation and that this approach is better than antiarrhythmic drug to control the rhythm. However, there has not been any long-term study to determine whether catheter ablation to abolish atrial fibrillation in heart failure patients would reduce mortality or admissions for heart failure.
This study is to compare the effect of catheter ablation-based atrial fibrillation rhythm control to rate control in patients with heart failure and high burden atrial fibrillation on the composite endpoint of all-cause mortality and heart failure events defined as an admission to a healthcare facility for > 24 hours or clinically significant worsening heart failure leading to an intervention (defined as treatment in an emergency department, a same-day access clinic, or an infusion centre) or unscheduled visits to a healthcare provider for administration of an intravenous diuretic and an increase in chronic heart failure therapy. This study may have a dramatic impact on the way the investigators manage these patients with atrial fibrillation and heart failure and may improve the outlook and well being of these patients.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Substudy_ In a subset of patients, following informed consent, additional data collection will include annual NT-proBNP/BNP measurements, Echocardiogram baseline and annually and 14 Day ECG Continuous Monitoring at six month intervals.
Updated June 2024:
Additional analysis will be completed using the winratio analysis for the hierarchical primary outcome of:
- All-cause mortality (time to event)
- Heart Failure Events (number of events per year) defined as an admission to a healthcare facility for > 24 hours or clinically significant worsening heart failure leading to an intervention (defined as treatment in an emergency department, a same-day access clinic, or an infusion centre) or unscheduled visits to a healthcare provider for administration of an intravenous diuretic as accepted by FDA, and an increase in chronic heart failure therapy
- Minnesota Living with Heart Failure Questionnaire (change from baseline to 12-month)
- Six Minute Hall Walk Test (change from baseline to 12-month)
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Rio Grande do Sul
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Porto Alegre, Rio Grande do Sul, Brasil, 90620-001
- Instituto de Cardiologia-FUC RS
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Alberta
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Calgary, Alberta, Canadá, T2N 2T9
- Libin Cardiovascular Institute of Alberta, Calgary
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Edmonton, Alberta, Canadá, T5H 3V9
- Royal Alexandra Hospital
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British Columbia
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Vancouver, British Columbia, Canadá, V6Z 1Y6
- Vancouver General
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Victoria, British Columbia, Canadá, V8R 4R2
- Royal Jubilee Hospital
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Nova Scotia
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Halifax, Nova Scotia, Canadá, B3H 3A7
- Queen Elizabeth II Health Science
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Ontario
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Hamilton, Ontario, Canadá, L8L 2X2
- Hamilton Health Sciences Centre
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Kingston, Ontario, Canadá, K7L 2V7
- Kingston General Hospital
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Kitchener, Ontario, Canadá, N2M 1B2
- St. Mary's General Hospital
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London, Ontario, Canadá, N6A 5A5
- London Health Sciences Centre
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Newmarket, Ontario, Canadá, L3Y 8C3
- Southlake Regional Health Care
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Ottawa, Ontario, Canadá, K1Y 4W7
- University of Ottawa Heart Institute
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Toronto, Ontario, Canadá, M4N 3M5
- Sunnybrook Health Sciences Centre
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Toronto, Ontario, Canadá, M5G 2M9
- Toronto General Hospital, University Health Network
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Quebec
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Montreal, Quebec, Canadá, H3A 1A1
- McGill University Health Centre
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Montreal, Quebec, Canadá, H1T 1C8
- Institute de Cardiologie de Montréal
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Montreal, Quebec, Canadá, H2L 4M1
- CHUM Centre hospitalier universitaire de Montréal
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Québec, Quebec, Canadá, G1V 4G5
- Insitut universitaire de cardiologie and pneumologie de Quebec
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Sherbrooke, Quebec, Canadá, J1H 5N4
- CHUS Centre Hospitalier Universitaire de Sherbrooke
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Stockholm, Suecia, S-171 76
- Karolinska University Hospital
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Taipei, Taiwán, 100
- National Taiwan University Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
Patients with one of the following AF categories and at least one ECG documentation of AF
- High burden Paroxysmal defined as ≥ 4 episodes of AF in the last 6 months, and at least one episode > 6 hours (and no episode requiring cardioversion and no episode > 7 days)
- Persistent AF (1) defined as ≥ 4 episodes of AF in the last 6 months, and at least one episode > 6 hours, and at least one AF episode less than 7 days but requires cardioversion. No AF episodes are > 7 days
- Persistent AF (2) as defined by at least one episode of AF > 7 days but not > 1 year
- Long term persistent AF defined as an AF episode, at least one year in length and no episodes > 3 years
- Optimal therapy for heart failure of at least 6 weeks (according to 2009 ACCF/AHA class 1 recommendations).
- HF with NYHA class II or III symptoms with either impaired LV function (LVEF ≤ 45%) as determined by EF assessment within the previous 12 months or preserved LV function (LVEF > 45%) determined by by EF assessment within the previous 12 months
NT-pro BNP measures:
A) Patient has been hospitalized for Heart Failure* in the past 9 months, has been discharged AND:
i- Is presently in Normal Sinus Rhythm and NT-pro BNP is ≥ 400 pg/mL
ii- Is presently in Atrial Fibrillation and NT-pro BNP is ≥ 600 pg/mL
OR
B) Patient has had no hospitalization for Heart Failure in the past 9 months AND:
i- Has had paroxysmal Atrial Fibrillation, is presently in Normal Sinus Rhythm and NT-proBNP is ≥ 600 pg/mL
ii- Is presently in Atrial Fibrillation and NT-proBNP is ≥ 900 pg/mL
*Heart Failure Admission is defined as admission to hospital > 24 hours and received treatment for Heart failure
- Suitable candidate for catheter ablation or rate control therapy for the treatment of AF
- Age ≥18
Exclusion Criteria:
- Have an LA dimension > 55 mm as determined by an echocardiography within the previous year
- Had an acute coronary syndrome or coronary artery bypass surgery within 12 weeks
- Have rheumatic heart disease, severe aortic or mitral valvular heart disease using the AHA/ACC guidelines
- Have congenital heart disease including previous ASD repair, persistent left superior vena cava
- Had prior surgical or percutaneous AF ablation procedure or atrioventricular nodal (AVN) ablation
- Have a medical condition likely to limit survival to < 1 year
- Have New York Heart Association (NYHA) class IV heart failure symptoms
- Have contraindication to systematic anticoagulation
- Have renal failure requiring dialysis
- AF due to reversible cause e.g. hyperthyroid state
- Are pregnant
- Are included in other clinical trials that will affect the objectives of this study
- Have a history of non-compliance to medical therapy
- Are unable or unwilling to provide informed consent
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: Rhythm Control
Patients randomized to catheter ablation-based AF rhythm control group will receive optimal Heart Failure therapy and one or more aggressive catheter ablation, which include PV antral ablation and LA substrate ablation with or without adjunctive antiarrhythmic drug.
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Patients randomized to catheter ablation-based AF rhythm control group will receive optimal HF therapy and one or more aggressive catheter ablation, which include PV antral ablation and LA substrate ablation with or without adjunctive antiarrhythmic drug
Otros nombres:
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Comparador activo: Rate Control
Patients in the rate control group will receive optimal Heart Failure therapy and rate control measures to achieve a resting HR < 80 bpm and 6-minute walk HR < 110 bpm.
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Patients in the rate control group will receive optimal HF therapy and rate control measures to achieve a resting HR < 80 bpm and 6-minute walk HR < 110 bpm.
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Composite of All-cause Mortality and Heart Failure Events
Periodo de tiempo: Baseline to study completion, an average of 24 months
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Heart failure event defined as an admission to a healthcare facility for > 24 hours or clinically significant worsening heart failure leading to an intervention (defined as treatment in an emergency department, a same-day access clinic, or an infusion centre) or unscheduled visits to a healthcare provider for administration of an intravenous diuretic as accepted by FDA and an increase in chronic heart failure therapy
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Baseline to study completion, an average of 24 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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All-cause mortality
Periodo de tiempo: Baseline to a minimum of 24 months
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All-cause mortality
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Baseline to a minimum of 24 months
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Heart Failure events
Periodo de tiempo: Baseline to a minimum of 24 months
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Heart failure event defined as an admission to a healthcare facility for > 24 hours or clinically significant worsening heart failure leading to an intervention (defined as treatment in an emergency department, a same-day access clinic, or an infusion centre) or unscheduled visits to a healthcare provider for administration of an intravenous diuretic as accepted by FDA and an increase in chronic heart failure therapy
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Baseline to a minimum of 24 months
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Health related QoL
Periodo de tiempo: Baseline to a minimum of 24 months
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Minnesota Living with Heart Failure.
Scoring: The higher the score, the worse the HRQL
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Baseline to a minimum of 24 months
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Health related QoL
Periodo de tiempo: Baseline to a minimum of 24 months
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EuroQol- 5 Dimension.
Scoring 0 = worst to 100 = best
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Baseline to a minimum of 24 months
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Health related QoL
Periodo de tiempo: Baseline to a minimum of 24 months
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Atrial Fibrillation Effect on Quality-of-life.
Scoring 0 = worst to 100 = best
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Baseline to a minimum of 24 months
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Exercise capacity
Periodo de tiempo: Baseline to a minimum of 24 months
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as determined by 6 Minute Hall walk distance
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Baseline to a minimum of 24 months
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NT-proBNP/BNP at 1 year and at 2 year follow-up
Periodo de tiempo: Baseline to a minimum of 24 months
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NT-proBNP/BNP
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Baseline to a minimum of 24 months
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All-cause mortality and heart failure events in patients with HF, impaired (LVEF≤45%) LV function and high burden AF
Periodo de tiempo: Baseline to a minimum of 24 months
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Baseline to a minimum of 24 months
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All-cause mortality and heart failure events in patients with HF, preserved (LVEF > 45%) LV function and high burden AF
Periodo de tiempo: Baseline to a minimum of 24 months
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Baseline to a minimum of 24 months
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Health economics
Periodo de tiempo: Baseline to a minimum of 24 months
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Cost economics
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Baseline to a minimum of 24 months
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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LV function and remodeling (LVESVi) at 1 year and 2 year follow-up
Periodo de tiempo: Baseline to a minimum of 24 months
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Echocardiogram measure LVESVi
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Baseline to a minimum of 24 months
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AF Burden at 1 year and 2 year follow-up
Periodo de tiempo: Baseline to a minimum of 24 months
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14 Day Continuous ECG monitoring
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Baseline to a minimum of 24 months
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Total number of heart failure events
Periodo de tiempo: Baseline to a minimum of 24 months
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Heart failure event defined as an admission to a healthcare facility for > 24 hours or clinically significant worsening heart failure leading to an intervention (defined as treatment in an emergency department, a same-day access clinic, or an infusion centre) or unscheduled visits to a healthcare provider for administration of an intravenous diuretic as accepted by FDA and an increase in chronic heart failure therapy
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Baseline to a minimum of 24 months
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Total number of Cardiovascular hospitalizations
Periodo de tiempo: Baseline to a minimum of 24 months
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Cardiovascular hospitalizations
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Baseline to a minimum of 24 months
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Safety (Adverse Events)
Periodo de tiempo: Baseline to a minimum of 24 months
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Thromboembolic events, symptomatic Pulmonary vein stenosis, atrio-esophageal fistula, pericardial effusion requiring pericardiocentesis, major bleeding requiring blood transfusion, amiodarone induced thyroid, pulmonary and other toxicity
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Baseline to a minimum of 24 months
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Anthony Tang, MD FRCPC, Western University
- Investigador principal: George Wells, PhD, Ottawa Heart Institute Research Corporation
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimado)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades cardiovasculares
- Procesos Patológicos
- Enfermedades cardíacas
- Arritmias Cardiacas
- Condiciones Patológicas, Signos y Síntomas
- Insuficiencia cardiaca
- Fibrilación auricular
- Terapéutica
- Técnicas y procedimientos de diagnóstico
- Diagnóstico
- Procedimientos quirúrgicos, operativo
- Fenómenos fisiológicos circulatorios y respiratorios
- Examen físico
- Técnicas de ablación
- Ablación por radiofrecuencia
- Terapia con radiofrecuencia
- Signos vitales
- Hemodinámica
- Fenómenos fisiológicos cardiovasculares
- Ablación del catéter
- Ritmo cardíaco
Otros números de identificación del estudio
- 231888
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