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CEST-PROTECT: Proximal Flow Control With a Balloon Guide Catheter Plus Distal Embolic Protection: a Randomised, Open-label Trial Evaluating Cerebral Protection Techniques (CEST-PROTECT)

2026年9月20日 更新者:Xuanwu Hospital, Beijing

Balloon Guide Catheter-Mediated Proximal Flow Control Plus Distal Embolic Protection Versus Distal Embolic Protection Alone During Carotid Artery Stenting in Patients With Complex High-Risk Carotid Stenosis-A Multicentre, Randomised, Open-Label, Blinded Trial

This randomized controlled trial aims to evaluate whether a proximal-distal dual cerebral protection strategy can reduce the occurrence of new cerebral ischemic lesions compared with a single cerebral protection strategy in patients undergoing carotid artery stenting. Eligible participants will be randomly assigned to receive either dual cerebral protection using proximal flow control combined with a distal embolic protection device or conventional single cerebral protection. Brain magnetic resonance imaging will be performed after the procedure to assess new ischemic lesions. The study will also evaluate peri-procedural neurological events and other safety and efficacy outcomes.

研究概览

详细说明

Carotid artery stenting is an established treatment for selected patients with carotid artery stenosis, but peri-procedural cerebral embolization remains an important concern. Distal embolic protection devices are commonly used during carotid artery stenting; however, embolization may occur during lesion crossing or device manipulation before complete distal protection is established.

The CEST-PROTECT trial is a prospective, multicenter, randomized controlled study designed to investigate whether a proximal-distal dual cerebral protection strategy provides additional cerebral protection compared with a conventional single protection strategy during carotid artery stenting. Participants will be randomly assigned to the dual-protection group or the single-protection group.

In the dual-protection group, proximal flow control will be combined with a distal embolic protection device during carotid artery stenting. In the single-protection group, carotid artery stenting will be performed using conventional distal embolic protection alone.

Brain magnetic resonance imaging, including diffusion-weighted imaging, will be performed after the procedure to identify new cerebral ischemic lesions. Clinical neurological outcomes, procedural outcomes, and safety events will also be assessed during follow-up. The study is intended to determine whether the dual-protection strategy can reduce peri-procedural cerebral embolic injury without increasing procedure-related complications.

研究类型

介入性

注册 (估计的)

500

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100053
        • Xuanwu Hospital, Capital Medical University
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 80年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age 18 to 80 years, regardless of sex.
  2. Symptomatic carotid artery stenosis ≥50% or asymptomatic carotid artery stenosis ≥70%, with the degree of stenosis determined according to the prespecified NASCET method and confirmed by CTA, DSA, or MRA.
  3. Presence of at least one protocol-defined complex high-risk carotid stenosis feature confirmed by carotid ultrasonography, CTA, DSA, HR-VWI, or other protocol-specified imaging modalities.
  4. Written informed consent provided by the participant or legally authorized representative.

Exclusion Criteria:

  1. Other cerebrovascular lesions that may substantially increase peri-procedural risk or interfere with assessment of the primary outcome, including an untreated ipsilateral intracranial aneurysm >5 mm, cerebral arteriovenous malformation, dural arteriovenous fistula, or other vascular lesions considered to pose significant risk by multidisciplinary assessment.
  2. Severe ipsilateral intracranial tandem stenosis ≥70% that is related to a recent ischemic event, is planned for intervention during the study follow-up period, or may interfere with attribution of post-procedural stroke; or complete occlusion of the contralateral internal carotid artery with an unacceptable risk of intolerance to proximal flow arrest.
  3. Technical conditions precluding carotid artery stenting or preventing safe implementation of either randomized cerebral protection strategy, including target-vessel occlusion or near-occlusion with distal collapse; free-floating thrombus or high-burden active intraluminal thrombus; absence of an appropriate landing zone for the distal embolic protection device or balloon flow-control segment in the common carotid artery; inability to safely cross, deploy, or retrieve the distal protection device; inability to safely and stably position the balloon guide catheter; severe aortic arch, supra-aortic, carotid-origin, or iliofemoral disease resulting in unacceptable transfemoral access risk; severe vascular tortuosity, angulation, or calcification resulting in unacceptable device-passage, vascular-injury, or stent-deployment risk; unacceptable risk of intolerance to proximal flow arrest; or any other condition preventing safe implementation of either randomized strategy.
  4. Previous stenting, angioplasty, or other endovascular mechanical treatment of the target carotid artery; or carotid lesions not prespecified for inclusion in the etiologic complex-lesion cohort, including carotid dissection, vasculitis, traumatic or infectious lesions, pseudoaneurysm, or fibromuscular dysplasia other than carotid web.
  5. Modified Rankin Scale (mRS) score ≥3 after a recent stroke, or the presence of a large cerebral infarction, significant cerebral edema or mass effect, hemorrhagic transformation, impaired consciousness, progressive neurological deficits, or clinically unstable neurological status.
  6. Contraindication to contrast agents, antiplatelet therapy, anticoagulant therapy, or medications required during the procedure that cannot be adequately managed; or inability or expected inability to receive or complete protocol-required dual antiplatelet therapy.
  7. A recent ischemic event considered primarily cardioembolic, or the presence of a high-risk cardiac source of embolism such as left atrial or left ventricular thrombus, infective endocarditis, a mechanical heart valve with inadequate anticoagulation, or an intracardiac mass. Atrial fibrillation alone is not an absolute exclusion criterion unless it is considered the primary cause of the qualifying ischemic event or required anticoagulation cannot be safely combined with the protocol-required antiplatelet regimen.
  8. A serious medical condition precluding elective carotid artery stenting, including active bleeding, uncorrectable coagulopathy, severe renal dysfunction without adequate risk-control measures, persistent uncontrolled severe hypertension, active severe infection, myocardial infarction within 6 weeks before screening, unstable acute coronary syndrome, decompensated heart failure, uncontrolled severe arrhythmia, or another serious systemic disease.
  9. Contraindication to MRI or anticipated inability to complete the protocol-required baseline and post-procedural MRI/DWI examinations.
  10. Current participation, or participation within 3 months before screening, in another clinical study that may affect the study intervention, safety assessment, or primary outcome evaluation; or planned major surgery or endovascular treatment during the peri-procedural period or 30-day follow-up that may interfere with assessment of study outcomes.
  11. Inability to understand or comply with study procedures, provide valid informed consent, complete the 30-day clinical follow-up or neurological assessments, or provide reliable primary outcome data; or life expectancy shorter than the required study follow-up period.
  12. Any other condition that, in the investigator's judgment, makes the participant unsuitable for the study, substantially increases study-related risk, or may compromise the reliability of the study results.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:BGC proximal flow control plus distal filter embolic protection device

Carotid artery stenting will be performed via a transfemoral approach. Proximal flow control will be established using a balloon guide catheter (BGC) and combined with a distal filter embolic protection device, allowing the procedure to be performed under dual proximal and distal cerebral protection

Carotid artery stenting will be performed via a transfemoral approach. Proximal flow control will be established using a balloon guide catheter (BGC) and combined with a distal filter embolic protection device. Carotid artery stenting will then be completed under dual proximal and distal cerebral protection.

有源比较器:Single distal filter embolic protection device

Carotid artery stenting will be performed according to a standardized procedure under the protection of a distal embolic protection device. The selection criteria for the distal protection device and stent will be consistent with those used in the experimental group. The brand, model, size, rationale for selection, and details of device use will be fully documented.

Carotid artery stenting will be performed according to a standardized procedure under the protection of a distal embolic protection device. The selection criteria for the distal protection device and stent will be consistent with those used in the experimental group. The brand, model, size, rationale for selection, and details of device use will be fully

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Proportion of Participants With at Least One New Ipsilateral Cerebral Ischemic Lesion on Diffusion-Weighted MRI
大体时间:Within 72 hours after carotid artery stenting

The primary outcome is the proportion of participants with at least one new cerebral ischemic lesion on the side of the target carotid artery detected by diffusion-weighted magnetic resonance imaging (DWI) after carotid artery stenting, compared with the pre-procedural baseline MRI. New ischemic lesions will be assessed by an independent central imaging core laboratory blinded to treatment allocation.

Within 72 hours after carotid artery stenting

次要结果测量

结果测量
措施说明
大体时间
Composite of Any Stroke or All-Cause Death Within 30 Days
大体时间:Within 30 (±7) days after carotid artery stenting

First occurrence of any stroke or all-cause death within 30 days after carotid artery stenting. Clinical events will be adjudicated by an independent Clinical Events Committee blinded to treatment allocation.

Within 30 (±7) days after carotid artery stenting
Number and Distribution of New Cerebral Ischemic Lesions on Diffusion-Weighted MRI
大体时间:Within 72 hours after carotid artery stenting

The number and distribution of new cerebral ischemic lesions detected on post-procedural diffusion-weighted MRI compared with the pre-procedural baseline MRI. Distribution of new ischemic lesions according to laterality (ipsilateral or contralateral to the target carotid artery) and vascular territory involvement (single or multiple vascular territories). Lesions will be assessed by an independent central imaging core laboratory blinded to treatment allocation.

Within 72 hours after carotid artery stenting
Characteristics of New Cerebral Ischemic Lesions on Diffusion-Weighted MRI
大体时间:Within 72 hours after carotid artery stenting

New cerebral ischemic lesions will be classified as cortical or subcortical. Lesions will also be categorized according to the maximum lesion diameter.

Within 72 hours after carotid artery stenting
Proportion of Participants With New Symptomatic or Asymptomatic Cerebral Infarction
大体时间:Within 30 (±7) days after carotid artery stenting

The proportions of participants with newly developed symptomatic cerebral infarction and newly developed asymptomatic cerebral infarction after carotid artery stenting will be assessed separately. Symptomatic cerebral infarction is defined as a new cerebral infarction associated with corresponding new neurological symptoms, whereas asymptomatic cerebral infarction is defined as a new cerebral infarction without corresponding new neurological symptoms.

Within 30 (±7) days after carotid artery stenting
Incidence of Ipsilateral Ischemic Stroke
大体时间:Within 7 (±2) and 30 (±7) days after carotid artery stenting

The incidences of ipsilateral ischemic stroke will be assessed individually.

Within 7 (±2) and 30 (±7) days after carotid artery stenting
Incidence of Ipsilateral TIA
大体时间:Within 7 (±2) and 30 (±7) days after carotid artery stenting

The incidences of ipsilateral TIA will be assessed individually.

Within 7 (±2) and 30 (±7) days after carotid artery stenting
Incidence of All-cause Death
大体时间:Within 7 (±2) and 30 (±7) days after carotid artery stenting

The incidences of all-cause death will be assessed individually.

Within 7 (±2) and 30 (±7) days after carotid artery stenting
NIHSS Score and Change From Baseline
大体时间:At 7 (±2) days or hospital discharge, whichever occurs first, and at 30 (±7) days after carotid artery stenting

Neurological impairment will be assessed using the National Institutes of Health Stroke Scale (NIHSS). The NIHSS score and its change from the pre-procedural baseline will be evaluated at 7 days or hospital discharge and again at 30 days after carotid artery stenting.

At 7 (±2) days or hospital discharge, whichever occurs first, and at 30 (±7) days after carotid artery stenting
Modified Rankin Scale Score and Change From Baseline
大体时间:At 30 (±7) days after carotid artery stenting

Functional status will be assessed using the modified Rankin Scale (mRS). The mRS score and its change from the pre-procedural baseline will be evaluated at 30 days after carotid artery stenting.

At 30 (±7) days after carotid artery stenting
Incidence of Intracranial Hemorrhage
大体时间:Within 72 hours after carotid artery stenting

The proportion of participants experiencing any intracranial hemorrhage after carotid artery stenting.

Within 72 hours after carotid artery stenting
Incidence of Adverse Events and Serious Adverse Events
大体时间:Within 30 (±7) days after carotid artery stenting

The proportion of participants experiencing any adverse event (AE) or serious adverse event (SAE) after carotid artery stenting.

Within 30 (±7) days after carotid artery stenting
Incidence of Device- or Procedure-Related Adverse Events
大体时间:Within 30 (±7) days after carotid artery stenting

The proportion of participants experiencing adverse events or serious adverse events considered related to the study device or study procedure.

Within 30 (±7) days after carotid artery stenting

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月1日

初级完成 (估计的)

2029年4月1日

研究完成 (估计的)

2029年5月1日

研究注册日期

首次提交

2026年9月20日

首先提交符合 QC 标准的

2026年9月20日

首次发布 (实际的)

2026年9月25日

研究记录更新

最后更新发布 (实际的)

2026年9月25日

上次提交的符合 QC 标准的更新

2026年9月20日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

Deidentified individual participant data will not be shared.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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