Emergency Stroke Unit for Acute Cerebrovascular Events ( ESU-ACE-B )
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: Emergency Stroke Unit based on 0.23-T MRI, Standard stroke unit adherent to guidelines.
- Кому может быть актуально
- Состояния в реестре: Ischemic Stroke, Acute. 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 →
Не всё понятно в терминах? Прочитайте наш гид для пациентов →
Официальное название
Emergency Stroke Unit for Acute Cerebrovascular Events--A Prospective, Multicenter, Week-wise Randomized, Controlled Trial ( ESU-ACE-B )
Обзор
To compare the door-to-puncture time of patients with hyperacute ischemic stroke (between 4.5-6 hours after the onset of symptoms) treated in a standard stroke unit adherent to guidelines versus treated in Emergency Stroke Unit (a new stroke unit based on low-field magnetic resonance imaging).
Подробное описание
Mechanical thrombectomy is an effective reperfusion therapy for patients with acute ischemic stroke due to large vessel occlusion. Faster door-to-puncture time (DPT) is associated with significantly better clinical outcomes. With the development of low-field magnetic resonance imaging, it is poised to play an increasingly significant role in the early diagnosis and management of acute ischemic stroke. This prospective, multicenter, week-wise randomized controlled trial will compare the door-to-puncture time of patients with hyperacute ischemic stroke (between 4.5-6 hours after the onset of symptoms) managed in a standard stroke unit adherent to guidelines versus managed in Emergency Stroke Unit (a new stroke unit based on low-field magnetic resonance imaging).
Вмешательства
- Комбинированный продукт Emergency Stroke Unit based on 0.23-T MRI
The participants with hyperacute ischemic stroke (between 4.5-6 hours after onset of symptoms) who are eligible to receive reperfusion therapy will be managed by Emergency Stroke Unit process based on low-field magnetic resonance imaging. - Комбинированный продукт Standard stroke unit adherent to guidelines
The participants with hyperacute ischemic stroke (between 4.5-6 hours after onset of symptoms) who are eligible to receive reperfusion therapy will be managed by standard stroke unit process adherent to guidelines.
Первичные конечные точки
- Door-to-puncture time [Срок оценки: Door-to-puncture time]
Вторичные конечные точки (12)
- The utility-weighted modified Rankin Scale (uw-mRS) at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- Ordinal (shift) analysis of modified Rankin Scale (mRS) at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- Excellent functional outcome (Modified Rankin Scale score, mRS 0-1) at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- Good functional outcome (Modified Rankin Scale score, mRS 0-2) at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- The time from symptoms onset to endovascular thrombectomy decision. [Срок оценки: The time from symptoms onset to endovascular thrombectomy decision.]
- The time from emergency department arrival to endovascular thrombectomy decision. [Срок оценки: The time from emergency department arrival to endovascular thrombectomy decision.]
- Door-to-reperfusion time [Срок оценки: Door-to-reperfusion time]
- Symptomatic intracranial hemorrhages (according to the ECASS III criteria) within 36 hours. [Срок оценки: within 36 hours.]
- Symptomatic intracranial hemorrhages (according to the ECASS III criteria) at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- Mortality at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- Adverse events at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
- Serious adverse events at 14±2 days (or at discharge, whichever occurs first). [Срок оценки: at 14±2 days (or at discharge, whichever occurs first).]
Критерии участия
Критерии включения
- Age ≥ 18 years;
- Can be treated between 4.5-6 hours of symptoms onset\*(\*Symptom onset is defined by the "last seen normal" principle);
- Presenting with ischemic stroke symptoms;
- Pre-stroke mRS score 0-1;
- Baseline NIHSS score ≥ 5;
- Eligible for endovascular thrombectomy;
- Informed consent signed.
Критерии исключения
- Baseline NIHSS score < 5;
- Unable to undergo MRI because of claustrophobia;
- Patients with cardiac pacemaker/brain pacemaker/insulin pump implantation;
- Definite contraindication for endovascular thrombectomy;
- Patients with postictal hemiparesis (Todd's paralysis) or those with concomitant neurological/psychiatric conditions who are unable or unwilling to cooperate;
- Pregnant women, nursing mothers, or reluctance to use effective contraceptive measures during the period of trial;
- Participation in other interventional randomized clinical trials within 3 months before enrollment;
- Patients deemed unsuitable for participation in this trial by the investigator or those for whom participation in this trial may result in greater risks.
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
- Beijing Tiantan Hospital, Capital Medical University — Пекин
Идентификаторы
NCT: NCT06492265 · KY2024-131-02-B