Carotid Revascularization for Radiation Induced Carotid Artery Stenosis

Официальное название

Outcomes of Carotid Revascularization for Patients With Radiation Induced Carotid Artery Stenosis in China

Обзор

Cervical radiotherapy (RT) has greatly reduced the mortality of patients with malignant head and neck tumors, which, however, causes a higher risk of carotid artery stenosis, namely, radiation-induced carotid artery stenosis (RICS) and results in a significant increased risk of ischemic stroke. The systematic review and meta-analysis conducted by our team showed carotid endarterectomy (CEA) can yield better results for these patients than carotid artery stenting (CAS), which was contrary to most previous clinical guidelines. A large-scale prospective study is needed to verify the results. We will conduct a prospective registry of RICS patients treated with CEA to evaluate both short-term safety and long-term efficacy outcomes in a Chinese population.

Вмешательства

• Процедура Carotid endarterectomy (CEA)
  Surgeons follow the contemporary guideline combined with their experience and preference in order to ultimately select what is best suited for the patient and choose between CEA and CAS. Patients will receive 100 mg of aspirin or 75 mg of clopidogrel daily starting from at least 72 h prior to the CEA procedure and continued receiving the medication indefinitely. General anesthesia is recommended for CEA, although the use of standard or eversion endarterectomy, and a shunt or patch, is left to th
• Процедура Carotid artery stenting (CAS)
  Surgeons follow the contemporary guideline combined with their experience and preference in order to ultimately select what is best suited for the patient and choose between CEA and CAS. Patients will be given 100 mg of aspirin plus 75 mg of clopidogrel daily for at least 3 days before the CAS procedure and for 90 days after the procedure. They will receive a daily dose of 100 mg aspirin or 75 mg clopidogrel thereafter. For the CAS procedure, local anaesthesia and predilation prior to stent plac

Первичные конечные точки

• Stroke or death within 1 month [Срок оценки: Within 1-month post-procedure]

Вторичные конечные точки (7)

• Stroke beyond 1 month within 1 year [Срок оценки: Beyond 1-month and within 1 year post-procedure]
• Death beyond 1 month within 1 year [Срок оценки: Beyond 1-month and within 1 year post-procedure]
• Stroke or death within 1 year [Срок оценки: Within 1 year post-procedure]
• Cranial nerve injury [Срок оценки: Within 1-month post-procedure]
• Carotid artery restenosis [Срок оценки: Within 1-year post-procedure]
• Functional outcome [Срок оценки: Within 1-year post-procedure]
• Other major complications [Срок оценки: Within 1-month post-procedure]

Критерии участия

Критерии включения

• Patients with carotid stenosis who had a history of radiotherapy for head and neck cancer. (The median interval between the completion of radiation therapy and development of carotid artery stenosis detected on imaging (or vascular intervention) was no less than 1 years to avoid non-related situations. The target area of the radiotherapy included at least the ipsilateral neck, including part of the carotid system. The internal carotid stenosis was confirmed by angiography, Duplex, 3D angio-CTA or angio-MRI, and stenosis was defined as > 50% based on North American Symptomatic Carotid Endarterectomy Trial criteria), with or without symptom. Patients with a transient ischaemic attack (TIA) or stroke within 6 months were defined as symptomatic. TIA was defined as a transient episode of neurological dysfunction (focal weakness/ language disturbance/transient monocular blindness/ requiring assistance to walk) caused by focal brain or retinal ischemia that lasts for at least 10 min but resolves within 24 h.)

Критерии исключения

• The patients treated for restenosis.
• Intracranial arteriovenous malformation or aneurysm
• Severe stenosis or occlusion of the ipsilateral intracranial artery
• Unstable angina, myocardial infarction (MI), or congestive heart failure in the last 6 months
• Uncorrectable coagulation abnormalities
• Uncontrolled diabetes mellitus defined as glucose > 300 mg/dL (16.67 mmol/L)
• Pregnant or in the perinatal period
• Severe concomitant disease with poor prognosis (life expectancy < 2 years)
• Intolerance or allergies to any of the study medications, such as aspirin or clopidogrel

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 · 2 центра

• Xuanwu Hospital, Capital Medical University — Пекин
• Guangdong Provincial People's Hospital — Гуанчжоу

Идентификаторы

NCT: NCT05134246 · CRICS

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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