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.
Przegląd badań
Status
Interwencja / Leczenie
Szczegółowy opis
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)
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Rio Grande do Sul
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Porto Alegre, Rio Grande do Sul, Brazylia, 90620-001
- Instituto de Cardiologia-FUC RS
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Alberta
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Calgary, Alberta, Kanada, T2N 2T9
- Libin Cardiovascular Institute of Alberta, Calgary
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Edmonton, Alberta, Kanada, T5H 3V9
- Royal Alexandra Hospital
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British Columbia
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Vancouver, British Columbia, Kanada, V6Z 1Y6
- Vancouver General
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Victoria, British Columbia, Kanada, V8R 4R2
- Royal Jubilee Hospital
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Nova Scotia
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Halifax, Nova Scotia, Kanada, B3H 3A7
- Queen Elizabeth II Health Science
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Ontario
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Hamilton, Ontario, Kanada, L8L 2X2
- Hamilton Health Sciences Centre
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Kingston, Ontario, Kanada, K7L 2V7
- Kingston General Hospital
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Kitchener, Ontario, Kanada, N2M 1B2
- St. Mary's General Hospital
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London, Ontario, Kanada, N6A 5A5
- London Health Sciences Centre
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Newmarket, Ontario, Kanada, L3Y 8C3
- Southlake Regional Health Care
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Ottawa, Ontario, Kanada, K1Y 4W7
- University of Ottawa Heart Institute
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Toronto, Ontario, Kanada, M4N 3M5
- Sunnybrook Health Sciences Centre
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Toronto, Ontario, Kanada, M5G 2M9
- Toronto General Hospital, University Health Network
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Quebec
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Montreal, Quebec, Kanada, H3A 1A1
- McGill University Health Centre
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Montreal, Quebec, Kanada, H1T 1C8
- Institute de Cardiologie de Montréal
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Montreal, Quebec, Kanada, H2L 4M1
- CHUM Centre hospitalier universitaire de Montréal
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Québec, Quebec, Kanada, G1V 4G5
- Insitut universitaire de cardiologie and pneumologie de Quebec
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Sherbrooke, Quebec, Kanada, J1H 5N4
- CHUS Centre Hospitalier Universitaire de Sherbrooke
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Stockholm, Szwecja, S-171 76
- Karolinska University Hospital
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Taipei, Tajwan, 100
- National Taiwan University Hospital
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Opis
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 studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Aktywny komparator: 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
Inne nazwy:
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Aktywny komparator: 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.
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Composite of All-cause Mortality and Heart Failure Events
Ramy czasowe: 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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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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All-cause mortality
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: Baseline to a minimum of 24 months
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Baseline to a minimum of 24 months
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Health economics
Ramy czasowe: 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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Inne miary wyników
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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LV function and remodeling (LVESVi) at 1 year and 2 year follow-up
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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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Współpracownicy i badacze
Współpracownicy
Śledczy
- Główny śledczy: Anthony Tang, MD FRCPC, Western University
- Główny śledczy: George Wells, PhD, Ottawa Heart Institute Research Corporation
Publikacje i pomocne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Szacowany)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
- Choroby układu krążenia
- Procesy patologiczne
- Choroby serca
- Zaburzenia rytmu serca
- Stany patologiczne, oznaki i objawy
- Niewydolność serca
- Migotanie przedsionków
- Lecznictwo
- Techniki i procedury diagnostyczne
- Diagnoza
- Procedury chirurgiczne, operacyjny
- Zjawiska fizjologiczne krążenia i oddechu
- Badanie fizyczne
- Techniki ablacji
- Ablacja częstotliwości radiowej
- Terapia częstotliwości radiowej
- Znaki życiowe
- Hemodynamika
- Zjawiska fizjologiczne sercowo -naczyniowe
- Ablacja cewnika
- Tętno
Inne numery identyfikacyjne badania
- 231888
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