Меню
Идёт набор NCT06560047

Danish Evaluation of Early Catheter Ablation for Atrial Fibrillation in Patients With Heart Failure

Без фазы С лечением Atrial Fibrillation Heart Failure

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Catheter ablation.
Кому может быть актуально
Состояния в реестре: Atrial Fibrillation, Heart Failure. Базовые параметры: 18 лет — 80 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Дания
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Danish Evaluation of Early Catheter Ablation for Atrial Fibrillation in Patients With Heart Failure - The DanAblate-HF Trial

Обзор

The DanAblate-HF trial will investigate whether early catheter ablation treatment for atrial fibrillation in patients with heart failure is superior to standard treatment.

Подробное описание

Atrial fibrillation (AF) is the most common arrhythmia in patients with heart failure (HF), with rates ranging between 20-65%, depending on age, severity of HF, subtypes of HF and duration of HF. The two conditions have an intricate and often overlapping pathophysiology, with each condition leading to development of the other, as well as progression of disease. Studies have shown that the presence of AF in HF patients is associated with increased morbidity and mortality, deterioration in HF, exacerbated HF symptoms, and reduced quality of life. The optimal treatment of AF in the presence of HF remains unknown. Currently, there is a pull towards catheter ablation as first-line therapy for AF in HF patients. However, there is no solid scientific evidence to support this approach. Furthermore, it is unknown whether early rhythm control by catheter ablation in HF patients is beneficial.

The investigators aim to conduct a pragmatic, randomized clinical trial designed to evaluate the efficacy and safety of early catheter ablation for AF in patients with HF compared with standard treatment.

Eligible patients with HF and AF will be prospectively screened from all Danish hospitals and randomized 1:1 to early catheter ablation with pulmonary vein isolation (within 6 weeks) or standard guideline directed treatment for AF. Patients with reversible causes for AF, conditions that preclude the use of catheter ablation or previous catheter ablation for AF will be excluded from the study. Randomization and follow-up will be conducted at six specialized sites in Denmark. There will be one scheduled on-site 12-months follow-up visit after randomization. All clinical follow-up will be conducted at the patient's local hospital, according to standard practice and out of trial setting. Information regarding hospital visits/admissions, events, adverse events, changes in medication, cross-over, heart rhythm and rate, and results of relevant blood-work will be ascertained through systematic patient chart-review at pre-specified time-points. The results from this trial will mold future treatment of AF in HF patients. The investigators hypothesize that early catheter ablation reduces the risk of HF hospitalizations and mortality when compared with standard treatment, thereby significantly improving the clinical prognosis for patients with HF and AF.

Вмешательства

  • Процедура Catheter ablation
    Catheter ablation with pulmonary vein isolation will be the study intervention. Patients randomized to the intervention arm will undergo catheter ablation within six weeks of randomization. In the waiting-time for ablation, patients will receive standard treatment for AF and HF, as per current guideline recommendations. Catheter ablation will be performed at one of six high-volume ablation centers in Denmark. Mode of catheter ablation will be at the discretion of the operator. Radiofrequency abl

Первичные конечные точки

  • Time to hospitalization for worsening HF or cardiovascular death [Срок оценки: From baseline to study completion, with a minimum of 1 year]
Вторичные конечные точки (12)
  • Time to cardiovascular death [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to all-cause mortality [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to first heart failure hospitalization [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to first-time AF hospitalization [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to primary outcome stratified by age [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to primary outcome stratified by sex [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to primary outcome stratified by symptomatic and asymptomatic AF [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to primary outcome stratified by paroxysmal or persistent AF [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Time to primary outcome stratified by left ventricular ejection fraction (LVEF) [Срок оценки: From baseline to study completion, with a minimum of 1 year]
  • Change in Quality of Life [Срок оценки: From baseline to 12 months]
  • Change in self-assessed health [Срок оценки: From baseline to 12 months]
  • Change in New York Heart Association (NYHA) class [Срок оценки: From baseline to 12 months]

Критерии участия

Критерии включения

  • HF patients with AF within the past 12 months

HF is defined as all of the below (all must apply)

  • Clinically assessed Heart Failure with Reduced Ejection Fraction (HFrEF)
  • An indication for initiation or ongoing guideline directed medical therapy for HFrEF, according to current Heart Failure guidelines
  • LVEF < 50% at any point during the past 12 months

AF is defined as one or more of the following:

A. Symptomatic AF, documented by ECG, Holter of CIED

B. Asymptomatic AF with one or more of the following:

  • Clinical indication for rhythm or rate control (documented by ECG, telemetry, Holter, CIED)
  • ≥2 ECG detected AF episodes within 3 months (on separate dates)
  • Holter detected AF with a continuous duration of more than 6 hours
  • CIED detected AF with continuous duration >24 hours
  • 18 years ≤ Age <80 years
  • Optimal medical therapy for HFrEF or planned/current uptitration in guideline directed medical therapy for HFrEF
  • Treatment with anticoagulation for stroke prevention, initiated according to guidelines for treatment of AF

Критерии исключения

  • Life-expectancy < 1 year
  • BMI > 40
  • Contraindications or unacceptable side effects to rate limiting drugs AND amiodarone
  • LA size (indexed for BSA) > 60 ml/m2 (volume) on echo within the last year
  • Documented persistent/permanent AF > 1 year
  • Previous AF ablation/surgery
  • Reversible causes of AF (including, but not limited to, infection within 14 days, untreated thyroid disease, surgery)
  • Severe valvular disease
  • Acute myocardial infarction, cardiothoracic surgery or stroke within the past 3 months
  • Planned cardiothoracic surgery
  • Listed for heart transplant
  • Contraindications for anticoagulation therapy or catheter ablation
  • Severe kidney disease (CKD≥5)
  • Pregnancy
  • Patient unwilling to try medical therapy for AF
  • Patient unwilling/unable to give informed consent for study participation

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Дания · 6 центров
  • Aalborg University Hospital, Department of Cardiology — Aalborg
  • Aarhus University Hospital — Aarhus
  • Department of Cardiology, Rigshospitalet — Copenhagen
  • Department of Cardiology, Herlev-Gentofte University Hospital — Hellerup
  • Department of Cardiology, Odense University Hospital — Odense
  • Department of Cardiology, Zealand University Hospital — Roskilde

Идентификаторы

NCT: NCT06560047 · N-20240001 · F2024-063

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗