Residual Stenosis and Restenosis Following Carotid Endarterectomy With Primary Closure, A Prospective Tracking 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
- Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
- Кому может быть актуально
- Состояния в реестре: Carotid Arteriosclerosis, Carotid Stenosis, Brain Stroke. Базовые параметры: 18 лет — 90 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
- Чехия
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
This prospective, multicenter observational study aims to evaluate the incidence, timing, and characteristics of residual and recurrent (restenosis) carotid artery stenosis following carotid endarterectomy (CEA) with primary closure. Conducted across several neurosurgical centers in the Czech Republic, the study will include patients undergoing elective CEA who meet standard clinical indications. Participants will undergo preoperative CT angiography and follow-up imaging at 30 days and 1 year post-surgery. Residual stenosis is defined as ≥50% luminal narrowing detected within 30 days postoperatively, while restenosis is evaluated at later time points. The study will also assess clinical outcomes such as ischemic stroke, TIA, myocardial infarction, and mortality. The standardized surgical technique and harmonized diagnostic algorithm across all centers aim to provide robust data on the performance and durability of primary closure CEA.
Подробное описание
Study Objective:
The objective of this study is to assess the true incidence of restenosis following CEA in the Czech Republic. A major advantage of this study is the use of standardized surgical procedures across participating centers, along with unified data collection methods and diagnostic algorithms.
Methodology:
Patient Cohort:
All patients meeting the current guideline indications for CEA will be enrolled.
Exclusion criteria include:
Age ≤18 or ≥90 years
Previous endarterectomy or stenting
Unsuitable vascular anatomy
High perioperative risk
Contralateral cranial nerve X or XII palsy
History of neck irradiation
Tandem carotid stenosis or intracranial vascular pathology (e.g., aneurysm or AVM)
Absence of signed informed consent
Collected data will include:
Epidemiologic risk factors: age, sex, diabetes, hypertension, dyslipidemia, metabolic syndrome, renal insufficiency, smoking, physical activity, weight, comorbidities
Laboratory markers: LDL, HDL, cholesterol, lipoprotein A, triglycerides, CKD-EPI, sedimentation rate, fibrinogen, INR (Quick test), APTT
Diagnostics:
All patients will undergo non-contrast brain CT. Carotid stenosis will be assessed by CT angiography performed within 3 months prior to surgery. In addition to stenosis severity, the degree of calcification will be classified as:
No calcification
Minimal
Partially calcified
Pronounced
Severe/unable to evaluate
Other vascular pathology will also be recorded. Follow-up imaging will be performed at 1 month and 1 year postoperatively. CT findings will be assessed by two independent reviewers.
Surgical Technique:
All patients will receive mono- or dual antiplatelet therapy, and 5,000 IU of heparin will be administered intraoperatively. Surgery may be performed under general anesthesia with electrophysiological monitoring or under local anesthesia, based on the surgeon's preference.
A longitudinal incision will be made anterior to the sternocleidomastoid muscle. The common carotid artery and its branches will be dissected and clamped. The internal carotid artery will be clamped distal to the most significant stenosis, as identified on preoperative CTA. The surgeon will incise through the tunica adventitia and media to expose and excise the atherosclerotic plaque. Any residual fragments will be removed, and the arterial wall will be closed using 6/0 suture.
Follow-Up:
Patients will continue on mono- or dual antiplatelet therapy. Mandatory follow-up CT angiography will be performed at 30 days and1 year. During follow-up, the following will be evaluated:
CTA findings
Overall patient condition
Incidence of ischemic stroke (iCMP), TIA, myocardial infarction, and death
Outcomes:
Primary Outcome:
Restenosis ≥50% at 12 months
Secondary Outcomes:
Residual stenosis ≥50% at 30 days
iCMP/TIA/death/MI
Change in modified Rankin Scale (mRS)
Первичные конечные точки
- Restenosis ≥50% at 12 months [Срок оценки: 12 months]
Вторичные конечные точки (3)
- Restenosis ≥50% [Срок оценки: 30 days]
- iCMP/TIA/death/MI [Срок оценки: 1 year]
- Change in modified Rankin Scale (mRS) [Срок оценки: 1 year]
Критерии участия
Критерии включения
Patients without matching any of exclusion criteria who underwent cartotid endarterectomy
Критерии исключения
Age ≤18 or ≥90 years
Previous endarterectomy or stenting
Unsuitable vascular anatomy
High perioperative risk
Contralateral cranial nerve X or XII palsy
History of neck irradiation
Tandem carotid stenosis or intracranial vascular pathology (e.g., aneurysm or AVM)
Absence of signed informed consent
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Чехия · 1 центр
- Central Military Hospital Prague — Prague
Идентификаторы
NCT: NCT07057297 · 108/19-31/2024