Study on the Preferences for PCI Implantation Devices Among Doctors and Patients
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: Questionnaire.
- Кому может быть актуально
- Состояния в реестре: Coronary Artery Disease, Percutaneous Coronary Intervention. 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 →
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Официальное название
Study on the Preferences for Percutaneous Coronary Intervention Implantation Devices Among Healthcare Providers and Patients With Coronary Artery Disease
Обзор
The contemporary percutaneous treatment of coronary artery disease typically involves initial lesion preparation with balloon angioplasty, followed by the deployment of a drug-eluting stent (DES) to provide an immediate scaffold and reduce the long-term risk of restenosis. However, stent implantation continues to present notable challenges, primarily due to the metallic scaffold left behind. Compared to DES, drug-coated balloons (DCB) provide a direct release of antiproliferative drugs into the vessel wall, preventing coronary restenosis after angioplasty and limiting the risk of stent-related events. DCBs are an established treatment option for in-stent restenosis and small vessels. However, the REC-CAGEFREE I trial demonstrated that a strategy of DCB angioplasty with rescue stenting did not achieve non-inferiority compared with the intended DES implantation in patients with de novo, non-complex coronary artery disease (CAD), irrespective of vessel diameter. Previous studies have mainly focused on the efficacy of PCI strategies in reducing adverse event rates, while less attention has been paid to patients' willingness regarding stent implantation. The AHA conducted a systematic review on depression and poor prognosis among patients with acute coronary syndrome (ACS), concluding that health organizations should consider depression as an official risk factor for poor prognosis after ACS. A prior study of patients with coronary artery disease after stent implantation found that their anxiety stemmed primarily from concerns about the stent's long-term effects and its impact on their social interaction. However, data regarding patients' preferences on the selection of DES or DCB is scarce, and whether the psychological impact would differ between DES- or DCB-treated patients is still unknown. This study aimed to investigate the preferences of patients, as well as medical staff, for DES or DCB-based PCI.
Вмешательства
- Другое Questionnaire
A questionnaire regarding the preference of DCB or DES-based PCI among patients with CAD and medical staff
Первичные конечные точки
- Maximum acceptable risk in the trade-off of death [Срок оценки: Before discharge]
- Maximum acceptable risk in the trade-off of stroke [Срок оценки: Before discharge]
- Maximum acceptable risk in the trade-off of myocardial infarction [Срок оценки: Before discharge]
- Maximum acceptable risk in the trade-off of cardiopulmonary resuscitation [Срок оценки: Before discharge]
- Maximum acceptable risk in the trade-off of revascularization [Срок оценки: Before discharge]
- Maximum acceptable risk in the trade-off of rehospitalization [Срок оценки: Before discharge]
Критерии участия
Критерии включения
- Patients with acute or chronic coronary syndrome who have undergone percutaneous coronary intervention;
- Patients who can understand the purpose of this trial and are willing to participate in the preference questionnaire.
- Healthcare providers who treat patients with coronary artery disease.
Критерии исключения
- Aged < 18 years;
- Inability to understand the questionnaire or presence of cognitive impairment.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Китай · 1 центр
- Xijing Hospital — Сиань
Идентификаторы
NCT: NCT07378163 · REC-DEVICEPREF