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Идёт набор NCT07601763

Pulsed Field Ablation Outcomes With Efficacy and Randomization in Atrial Fibrillation (POWER-AF)

Без фазы С лечением Atrial Fibrillation (AF) Atrial Fibrillation Ablation Atrial Fibrillation Recurrent Pulsed Field Ablation

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: Pulsed field ablation, Radiofrequency ablation alone, Pulsed field ablation system.
Кому может быть актуально
Состояния в реестре: Atrial Fibrillation (AF), Atrial Fibrillation Ablation, Atrial Fibrillation Recurrent, Pulsed Field Ablation. Базовые параметры: от 18 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
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Pulsed Field Ablation for Atrial Fibrillation Including Posterior Wall and Linear Ablation: A Randomized Controlled Trial of Safety and Efficacy (POWER-AF)

Обзор

Atrial fibrillation (AF) is one of the most common arrhythmias in clinical practice. As of 2019, there were approximately 59.7 million patients with AF worldwide, including atrial flutter (AF). Atrial fibrillation can significantly increase the risks of stroke, thromboembolism and heart failure in patients, seriously affecting their quality of life. Catheter ablation is the main means for rhythm control in patients with atrial fibrillation. A large number of clinical studies have confirmed the effectiveness and safety of catheter ablation for atrial fibrillation. It is significantly superior to drug treatment in maintaining sinus rhythm and can significantly improve symptoms and quality of life. Pulsed electric field ablation (PFA) is a novel ablation method that utilizes pulsed electric fields as energy. It uses multiple short-duration and high-voltage electrical pulses to release ablation energy, selectively causing myocardial cells to rupture and die. However, it has no obvious damaging effect on blood vessels, nerves, and tissues around the heart, such as the lungs, esophagus, and phrenic nerve. This trial was designed based on the advantage of the characteristic that PFA does not damage the esophagus, confining the damage to the posterior half of the left atrium and the circumferential isthmus of the mitral valve. While improving the ablation success rate, it is possible to protect the function of the left atrium. This study aims to verify the superiority of the new rhythm control strategy in a large-scale population by launching a prospective randomized controlled trial.

Вмешательства

  • Процедура Pulsed field ablation
    Left atrial electrical anatomical mapping modeling was performed using a high-density mapping catheter, and ablation was carried out using a pulsed field catheter. For patients with paroxysmal atrial fibrillation, bilateral large loop pulmonary vein isolation combined with left posterior atrial wall ablation is performed. For patients with persistent atrial fibrillation, bilateral large loop pulmonary vein isolation, left posterior atrial wall ablation, and mitral valve isthmus ablation are perf
  • Процедура Radiofrequency ablation alone
    Radiofrequency ablation will be performed using a saline perfusion catheter, and the ablation catheter was empirically selected by the surgeon. For patients with paroxysmal atrial fibrillation, circumferential pulmonary vein isolation is performed. For patients with persistent atrial fibrillation, circumferential pulmonary vein isolation combined with individualized linear ablation is performed. For those whose ablation of all the established routes has been completed but whose sinus rhythm has
  • Устройство Pulsed field ablation system
    Pulsed field ablation will be performed using a pulsed field ablation system for pulmonary vein isolation and additional ablation as clinically indicated.

Первичные конечные точки

  • Recurrence of atrial fibrillation within 12 months after ablation [Срок оценки: 12 months after ablation]
Вторичные конечные точки (5)
  • Change in atrial fibrillation burden from baseline to 12 months after ablation [Срок оценки: Baseline and 12 months after ablation]
  • Change in left ventricular ejection fraction from baseline to 12 months after ablation [Срок оценки: Baseline and 12 months after ablation]
  • Change in 36-Item Short Form Health Survey physical component summary score from baseline to 12 months after ablation [Срок оценки: Baseline and 12 months after ablation]
  • All-cause mortality within 12 months after ablation [Срок оценки: 12 months after ablation]
  • Change in 36-Item Short Form Health Survey mental component summary score from baseline to 12 months after ablation [Срок оценки: Baseline and 12 months after ablation]

Критерии участия

Критерии включения

  • Atrial fibrillation patients who will accept catheter ablation.
  • Age ≥ 18.
  • Be capable of understanding and signing the informed consent form.

Критерии исключения

  • Have contraindications for catheter ablation (such as atrial thrombosis, decompensated heart failure, etc.)
  • Have accepted catheter ablation before.
  • Myocardial infarction, or any cardiac interventional/surgery has been performed within 3 months.
  • Had a stroke or transient ischemic attack within 6 months.
  • Allergy to iodine contrast agents.
  • Participate in clinical trials related to other drugs or devices.
  • Pregnant women, lactating women, or women with plans to become pregnant shortly.
  • Active stage of infection.
  • Secondary atrial fibrillation, such as combined with rheumatic heart disease, hypertrophic cardiomyopathy, etc.
  • Patients who do not agree to be enrolled or are unable to cooperate to complete the study

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
Простое слепое
Основная цель
Лечение

Центры проведения

Китай · 1 центр
  • National Cardiovascular Diseases Center, Fuwai Hospital — Пекин

Идентификаторы

NCT: NCT07601763 · 2024-2569

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗