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EndovascularTherapy Versus Standard Medical Terapy for Intracranial Large Vessel Occlusion in 24 Hours to 30 Days

2026年9月21日 更新者:Xuan Sun

EndovascularTherapy Versus Standard Medical Terapy for Intracranial Large Vessel Occlusion in 24 Hours to 30 Days: A Prospective, Multicenter, Real-world Cohort Trial

This study is a prospective, multicenter, observational cohort study using a real-world study design. The aim of this study is to compare functional and safety outcomes of intravascular recanalization therapy (with COSIS distal stent protection technology strategy as the core) combined with standard drug therapy in improving functional outcomes in patients with intracranial large vessel occlusion in the ultra late window (24 hours-30 days) compared with standard drug therapy alone.

研究概览

详细说明

Patients with ischemic stroke whose onset or last known well (LKW) ranged from 24 hours to 30 days, who were confirmed by imaging to have intracranial large vessel occlusion and may still have brain tissue that can be saved were included. The study did not interfere with the choice of treatment options. Patients received intravascular therapy or standard drug treatment, which was determined by clinicians according to the condition, imaging characteristics and the joint decision of doctors and patients. According to the actual treatment of patients, the intravascular treatment cohort and the standard drug treatment cohort were formed, in which the intravascular treatment was centered on the COSIS distal stent protection strategy. The primary outcome is proportion of patients with functional independence defined as mRS score of 0-2 at 90 days after enrollment.

研究类型

观察性的

注册 (估计的)

150

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

  • 姓名:Xuan Sun, MD
  • 电话号码:13810926284
  • 邮箱:sxuan@yeah.net

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100070
        • Beijing Tiantan Hospitall, 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 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

取样方法

非概率样本

研究人群

All research centers continuously screened eligible patients according to unified standards. The study did not interfere with the choice of treatment options. Whether the patients received intravascular therapy was determined by clinicians according to the condition, imaging characteristics, treatment risk and the joint decision of doctors and patients.

This is a prospective multicenter observational registry-based cohort study. Endovascular treatment is a routine clinical interventional procedure. The decision whether to perform endovascular treatment is made by treating clinicians, not assigned by study investigators. Investigators only collect real-world clinical data and follow-up outcomes of enrolled participants.

描述

Inclusion Criteria:

  1. Age≥18 years
  2. The clinical diagnosis was ischemic stroke, and imaging confirmed the presence of intracranial large vessel occlusion
  3. The time from LKW or the time of finding symptoms is 24 hours to 72 hours; or more than 72 hours but not more than 30 days, and there are neurological deterioration or fluctuation
  4. Imaging findings suggest that there may still be salvageable brain tissue, which meets any of the following conditions: perfusion imaging examination shows that the ischemic core volume < 70 ml and the mismatch ratio > 1.2; CTA or DSA showed moderate or good collateral circulation; MRI-DWI showed a significant mismatch between lesion size and clinical symptoms
  5. The modified Rankin Scale score (mRS) before onset was 0-1
  6. The subjects themselves or their legal representatives voluntarily participated in the study and signed written informed consent

Exclusion Criteria:

  1. Large area cerebral infarction or imaging showed obvious space occupying effect, such as ASPECTS<6 points,or brainstem infarction area exceeded 1/3 of the corresponding anatomical area
  2. Isolated extracranial carotid or vertebral artery occlusion
  3. Intracranial tumors, arteriovenous malformations or other serious intracranial diseases that may significantly affect the evaluation of the outcome of the study
  4. Intracranial hemorrhage occurred in the past 3 months
  5. There is a risk of severe coagulation dysfunction, active bleeding or other high bleeding that cannot be corrected
  6. Severe liver and kidney function damage, which may affect treatment or follow-up
  7. Pregnant or lactating women
  8. The estimated survival time is less than 1 year
  9. Unable to complete 90-day clinical follow-up or main outcome assessment
  10. Participating in other interventional clinical trials that may affect the treatment or outcome evaluation of this study
  11. Other circumstances that the researcher believes are not suitable for participating in this study

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

  • 观测模型:COHORT
  • 时间观点:PROSPECTIVE

队列和干预

团体/队列
干预/治疗
Endovascular Treatment Cohort

Intravascular therapy combined with standard drug therapy, in which the core of intravascular therapy is the cosis distal stent protection strategy.

The recanalization strategy with COSIS distal stent protection technology as the core was used in endovascular treatment.In addition to thrombus removal, the device mainly uses its distal closed basket structure and stent guide wire to form protection and anchor fulcrum at the distal end of occlusion, so as to assist in balloon dilatation, thrombus removal or stent implantation of complex occlusive lesions, and reduce thrombus escape.

Standard Medical Therapy Cohort

Standard drug therapy alone.It mainly includes antiplatelet therapy or anticoagulation therapy, lipid-lowering therapy, blood pressure and blood glucose management, etc.

Standard drug therapy is implemented in accordance with the current guidelines for the diagnosis and treatment of cerebrovascular diseases and the routine of each center, mainly including antiplatelet or anticoagulation therapy, lipid-lowering therapy, blood pressure and blood glucose management, etc.

The drug name, dose, route of administration, frequency of administration and course of treatment are determined by the clinician according to the patient's condition. The study only recorded the actual drug treatment and important adjustments.

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
The proportion of patients with functional independence defined as mRS score of 0 - 2 at 90 days after enrollment
大体时间:90 days after enrollment

The modified Rankin scale (mRS) ranged from 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability,5 severe disability, and 6 death.

90 days after enrollment

次要结果测量

结果测量
措施说明
大体时间
The overall distribution of mRS at 90 days after enrollment
大体时间:90 days after enrollment

The modified Rankin scale (mRS) ranged from 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability,5 severe disability, and 6 death.

90 days after enrollment
National Institutes of Health Stroke Scale (NIHSS) score 24 hours after treatment
大体时间:24 hours after treatment

The National Institute of Health Stroke Scale (NIHSS) ranged from 0 to 42, with higher scores indicating greater neurologic deficits.

24 hours after treatment
National Institutes of Health Stroke Scale (NIHSS) score at discharge
大体时间:At discharge

The National Institute of Health Stroke Scale (NIHSS) ranged from 0 to 42, with higher scores indicating greater neurologic deficits.

At discharge
National Institutes of Health Stroke Scale (NIHSS) score 30 days after enrollment
大体时间:30 days after enrollment

The National Institute of Health Stroke Scale (NIHSS) ranged from 0 to 42, with higher scores indicating greater neurologic deficits.

30 days after enrollment
National Institutes of Health Stroke Scale (NIHSS) score 90 days after enrollment
大体时间:90 days after enrollment

The National Institute of Health Stroke Scale (NIHSS) ranged from 0 to 42, with higher scores indicating greater neurologic deficits.

90 days after enrollment
The recurrence rate of stroke within 90 days after enrollment
大体时间:90 days after enrollment

The recurrence rate of stroke within 90 days after enrollment.

90 days after enrollment
Transient ischemic attack within 90 days after enrollment
大体时间:90 days after enrollment

Transient ischemic attack within 90 days after enrollment.

90 days after enrollment
All-cause mortality within 90 days after enrollment
大体时间:90 days after enrollment

All-cause mortality within 90 days after enrollment.

90 days after enrollment
Revascularization of target vessels within 90 days after enrollment
大体时间:90 days after enrollment

Revascularization of target vessels within 90 days after enrollment.

90 days after enrollment
The technical success rate of the intravascular treatment cohort,successful recanalization of the target vessel with residual stenosis <50% and final mTICI grade≥2b
大体时间:At the end of the procedure

The technical success rate of the intravascular treatment cohort,successful recanalization of the target vessel with residual stenosis <50% and final mTICI grade≥2b.

At the end of the procedure
Degree of recanalization in the intravascular treatment cohort
大体时间:At the end of the procedure

Degree of recanalization in the intravascular treatment cohort.The mTICI scale evaluates angiographic recanalization after endovascular therapy for acute ischemic stroke. Grades range from 0 (no perfusion) to 3 (complete recanalization). mTICI grade≥2b is defined as successful recanalization.

At the end of the procedure
Operation time of intravascular treatment cohort
大体时间:During the procedure

Operation time of intravascular treatment cohort.

During the procedure
Distribution of mRS scores at 6 months after enrollment
大体时间:6 months after enrollment

The modified Rankin scale (mRS) ranged from 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability,5 severe disability, and 6 death.

6 months after enrollment
The recurrence rate of stroke at 6 months after enrollment
大体时间:6 months after enrollment

The recurrence rate of stroke at 6 months after enrollment.

6 months after enrollment
Transient ischemic attack at 6 months after enrollment
大体时间:6 months after enrollment

Transient ischemic attack at 6 months after enrollment.

6 months after enrollment
All-cause mortality at 6 months after enrollment
大体时间:6 months after enrollment

All-cause mortality at 6 months after enrollment.

6 months after enrollment
Revascularization of target vessels at 6 months after enrollment
大体时间:6 months after enrollment

Revascularization of target vessels at 6 months after enrollment.

6 months after enrollment
Distribution of mRS scores at 12 months after enrollment
大体时间:12 months after enrollment

The modified Rankin scale (mRS) ranged from 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability,5 severe disability, and 6 death.

12 months after enrollment
The recurrence rate of stroke at 12 months after enrollment
大体时间:12 months after enrollment

The recurrence rate of stroke at 12 months after enrollment.

12 months after enrollment
Transient ischemic attack at 12 months after enrollment
大体时间:12 months after enrollment

Transient ischemic attack at 12 months after enrollment.

12 months after enrollment
All-cause mortality at 12 months after enrollment
大体时间:12 months after enrollment

All-cause mortality at 12 months after enrollment.

12 months after enrollment
Revascularization of target vessels at 12 months after enrollment
大体时间:12 months after enrollment

Revascularization of target vessels at 12 months after enrollment.

12 months after enrollment

其他结果措施

结果测量
措施说明
大体时间
Adverse events within 12 months after enrollment
大体时间:12 months after enrollment

Adverse events events within 12 months after enrollment.

12 months after enrollment
Serious adverse events within 12 months after enrollment
大体时间:12 months after enrollment

Serious adverse events within 12 months after enrollment.

12 months after enrollment
Symptomatic intracranial hemorrhage within 12 months after enrollment
大体时间:12 months after enrollment

Symptomatic intracranial hemorrhage within 12 months after enrollment.

12 months after enrollment
Ischemic stroke within 12 months after enrollment
大体时间:12 months after enrollment

Ischemic stroke within 12 months after enrollment.

12 months after enrollment
Hemorrhagic stroke within 12 months after enrollment
大体时间:12 months after enrollment

Hemorrhagic stroke within 12 months after enrollment.

12 months after enrollment
All-cause death and other important clinical safety events within 12 months after enrollment
大体时间:12 months after enrollment

All-cause death and other important clinical safety events within 12 months after enrollment.

12 months after enrollment
Proportion of at least one complication in the intravascular therapy cohort
大体时间:Perioperative

The intravascular treatment cohort included perioperative vascular dissection, vascular perforation or rupture, distal embolization, acute occlusion, re-occlusion, cerebral hyperperfusion syndrome and puncture site complications.

Perioperative

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。

赞助

调查人员

  • 首席研究员:Xuan Sun, MD、Beijing Tiantan Hospital

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)

2028年12月31日

研究完成 (估计的)

2029年12月31日

研究注册日期

首次提交

2026年9月9日

首先提交符合 QC 标准的

2026年9月21日

首次发布 (实际的)

2026年9月28日

研究记录更新

最后更新发布 (实际的)

2026年9月28日

上次提交的符合 QC 标准的更新

2026年9月21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

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

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