Revascularization for Symptomatic Non-acute Carotid Artery Occlusion

Обзор

The short-term and long-term efficacy of recanalization therapy needs to be further confirmed by large-sample prospective studies. The comparison of success rate, complication rate and efficacy among the three recanalization modalities also needs to be further explored. The purpose of this cohort study is to observe the success rate, efficacy and safety of recanalization treatment for non-acute occlusion, and to further compare the advantages and disadvantages of CEA, endovascular intervention and hybrid surgery.

Подробное описание

Carotid artery occlusion is one of the primary causes of ischemic stroke. When the occlusion time exceeds 30 days, it is commonlly referred to as chronic carotid artery occlusion (CCAO), and patients with carotid artery occlusion over 24 hours are collectively referred as non-acute occlusion. Symptomatic non-acute occlusion patients with definite hemodynamic hypoperfusion still face a high risk of stroke recurrence under drug treatment, with recurrence rates reported to be between 12.3% and 22.7% within 2 years. Currently, the surgical methods for the treatment of carotid artery occlusion are mainly divided into extracranial-intracranial (EC-IC) bypass and recanalization treatment. Recanalization treatment includes CEA, endovascular intervention and hybrid surgery. While the Carotid Occlusion Surgery Study (COSS) and the recently published Carotid or Middle cerebral artery Occlusion Surgery Study (CMOSS) failed to reveal the significant advantages of EC-IC bypass surgery over medical treatment for patients with symptomatic artery occlusion combined with hemodynamic insufficiency, recanalization treatment has been shown to be a promising treatment modality by case-control studies with small sample size. However, the short-term and long-term efficacy of recanalization therapy needs to be further confirmed by large-sample prospective studies. The comparison of success rate, complication rate and efficacy among the three recanalization modalities also needs to be further explored. In addition, about half of non-acute occlusion patients have cognitive impairment, and the role of cerebral hemodynamics in cognitive impairment is still unclear. Therefore, the purpose of this cohort study is to observe the success rate, efficacy and safety of recanalization treatment for non-acute occlusion, and to further compare the advantages and disadvantages of CEA, endovascular intervention and hybrid surgery.

Вмешательства

• Процедура Carotid Endarterectomy (CEA)
  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, CAS and Hybrid Sugery. 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 endarte
• Процедура Carotid Artery Stenting (CAS)
  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, CAS and Hybrid Sugery. 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, general
• Процедура Hybrid Surgery
  Hybrid Surgery 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, CAS and Hybrid Sugery. Patients will be given 100 mg of aspirin plus 75 mg of clopidogrel daily for at least 5 days before the hybird surgery procedure. If they had stenting procedure, they will receive a daily dose of 100 mg aspirin and 75 mg clopidogrel thereafter. If not, they will take either 100mg as

Первичные конечные точки

• Stroke or death whthin 30 days or recurrent ischemic stroke related of qualifying artery beyond 30 days through 12 months [Срок оценки: Up to 12 months after procedure]
• MMSE within 30 and 90 days after procedure [Срок оценки: 30 days and 90 days after procedure]
• MoCA scale within 30 and 90 days after procedure [Срок оценки: 30 days and 90 days after procedure]

Вторичные конечные точки (8)

• Technical success rate [Срок оценки: Up to 24 hours after procedure]
• Procedural success rate [Срок оценки: Up to 24 hours after procedure]
• Any stroke within 30 days, 90 days and 12 months after procedure [Срок оценки: Within 30 days, 90 days and 12 months post-procedure]
• Death within 30 days, 90 days and 12 months after procedure [Срок оценки: Within30 days, 90 days and 12 months post-procedure]
• Cranial nerve injury [Срок оценки: Within 30 days and 90 days post-procedure]
• Carotid artery or internal carotid artery reocclusion [Срок оценки: Within 30 days, 90 days and 12 months post-procedure]
• Functional outcome [Срок оценки: Within 30 days and 90 days post-procedure]
• Other major complications [Срок оценки: Within 30 days, 90 days and 12 months post-procedure]

Критерии участия

Критерии включения

• Older than 18 years old;
• Sign the informed consent form;
• Carotid occlusion at least 24h;
• Patients with clinical localization symptoms: ipsilateral hemisphere ischemia symptoms or ipsilateral eye ischemia symptoms or cognition impairment, with or without anterior circulation blood supply area infarction;
• DSA confirmed common carotid artery or internal carotid artery (mTICI=0) occlusion;
• Perfusion imaging confirms the presence of hypoperfusion in the corresponding area(CBF decrease);
• The optimal medical treatment for patients who still have ischemic symptoms;
• Routine DWI and ADC sequence examinations are performed before surgery no new infarction;

Критерии исключения

• Intracranial arteriovenous malformation or aneurysm;
• Unstable angina, myocardial infarction (MI), or congestive heart failure in the last 6 months;
• Uncontrolled diabetes mellitus defined as glucose > 300 mg/dL (16.67 mmol/L);
• Patient is expected to have the ADP antagonist therapy interruption within 3 months after the procedure;
• Pregnant or in the perinatal period;
• Severe concomitant disease with poor prognosis (life expectancy < 3 years);
• Intolerance or allergies to any of the study medications, such as aspirin or clopidogrel;
• Allergy to iodine or radiographic contrast media;
• Concomitant vascular conditions precluding endovascular;
• Patients with large cerebral infarction within 2 weeks;
• History of ipsilateral vocal cord paralysis;
• Those with severe skin diseases who are expected to have difficulty healing the incision;
• Poor functional status before onset (mRS score 4-5 points).
• The area of infarction in the occluded vascular area exceeds half of the vascular supply area;
• Already have dementia or psychiatric illness and are unable to complete neurological and cognitive assessments.
• Any condition that in the surgeon's judgment suggests the patient an unsuitable surgical candidate.

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
• Xuanwu Hospital, Capital Medical University. — Пекин

Идентификаторы

NCT: NCT06303414 · RESCO

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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