COronary Re-engageMent aFter randOm NavitoR alignmenT (COMFORT STUDY)
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: TAVR Aligned, TAVR Random.
- Кому может быть актуально
- Состояния в реестре: Aortic Valve Stenosis, Transcatheter Aortic Valve Replacement. 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
- Италия
- 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
COronary Re-EngageMent aFter RandOm NavitoR Alignment (COMFORT STUDY)
Обзор
Whereas PCI before TAVR was previously recommended despite its uncertain prognostic role, recent data underline the possibility of a postponed coronary intervention using a commissural alignment technique. This approach allows easy coronary re-engagement through the valve stent frame with a trade off paid of procedure complexity. Considering the prevalence of coronary artery disease (CAD) and the increasing percentage of younger patients treated with TAVI, investigate whether a simpler procedure with random implantation of Navitor valve is not inferior in terms of coronary re-access, is required The key point of the project will be the evaluation of the feasibility of coronary re-engagement after a Navitor valve randomly implanted.
Подробное описание
Transcatheter Aortic Valve Implantation (TAVI) is recommended by European and American guidelines to treat patients with aortic stenosis regardless of procedural risk (1, 2). In the last decades the increasing percentage of younger patients treated with TAVI, reflect the extensive indications in lower risk setting, highlighting the importance of easy coronary re-engagement after valve implantation. Considering the prevalence and the progression of a pre-existing coronary artery disease (CAD), the timing of coronary intervention should be accurate selected (3) addressing the percentage of unplanned percutaneous coronary intervention (PCI) after TAVI (4). In fact, while PCI before TAVR was previously recommend despite the uncertain prognostic role (5), recent data remarks the possibility of a postponed coronary intervention using a commissural alignment technique (6) that allows a predictable stent frame position in the sinus of Valsalva (7). Moreover, following the emerging concept of easy re-access, only a few types of prostheses have been shown to have an high degree of stent position predictability after implantation, leading to a limited option in terms of prosthesis choice. Furthermore, to achieve the best results with commissural alignment technique, accurate procedure planning and operator's expertise are required in order to properly manage the valve specific orientation in the aorta with consequent increase in time, radiation and procedure complexity.
However, geometry of the stent frame (height and size) and the anatomical characteristics of patients have to be enlisted as contributory factors to difficult coronary re-engagement and need to be evaluate in order to establish the feasibility of the re-access after TAVR.
The investigators' findings could provide data regarding the non-inferiority rate of coronary cannulation after a simpler procedure with Navitor implantation without alignment technique. Due to these results, the valves portfolio available in patients with coronary artery disease that needed PCI after TAVR, could be larger and various allowing the best protheses choice according to the patient's anatomy and operator's expertise. Finally, knowing the predictors of difficult re-engagement for both types of valves, regardless of implantation technique, could be interesting for an even more valve tailored approach.
The purpose of this study is to investigate the feasibility of coronary re-engagement after randomly (not aligned) Navitor implantation, as already perform in current clinical practice, due to a lower predictable orientation of this type of valve.
Вмешательства
- Процедура TAVR Aligned
Investigate the feasibility of coronary re-engagement after commissural alignment technique in terms of success rate (%) and procedure complexity taking into account radiations, time and contrast used. - Процедура TAVR Random
TAVR Random Feasibility comparison of coronary re-engagement between the randomly implanted Navitor valve (unaligned) and the others implanted with the commissural alignment technique in terms of success rate (%) and complexity of the procedure, taking into account radiation, time and contrast used
Первичные конечные точки
- Coronary re-access after TAVR procedure [Срок оценки: During procedure]
Вторичные конечные точки (12)
- Total Implant Time [Срок оценки: During procedure]
- Total Implant Fluoroscopy Time [Срок оценки: During procedure]
- Total Implant Radiations [Срок оценки: During procedure]
- Total Implant Contrast [Срок оценки: During procedure]
- Alignment Radiation [Срок оценки: During procedure]
- Alignment Fluoroscopy Time [Срок оценки: During procedure]
- Implant Radiation [Срок оценки: During procedure]
- Implant Fluoroscopy Time [Срок оценки: During procedure]
- Implant Contrast [Срок оценки: During procedure]
- Re-Engagement Radiation [Срок оценки: During procedure]
- Re-Engagement Fluoroscopy Time [Срок оценки: During procedure]
- Re-Engagement Contrast used [Срок оценки: During procedure]
Критерии участия
Patients to be included in this registry should have all the following criteria:
1\. Severe, symptomatic aortic stenosis with an indication to TAVI
Exclusion criteria and definition
Patients excluded in this registry should have all the following criteria:
- Valve in Valve procedure
- Hemodynamical instability
- TAVR performed from other access (not femoral)
- No-CT Planned TAVR
- TAVR performed with Chimney Technique
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Италия · 1 центр
- ASST GOM Niguarda — Milan
Идентификаторы
NCT: NCT05779787 · D001024