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注册号: Registration number: |
ChiCTR2600125361 |
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最近更新日期: Date of Last Refreshed on: |
2026-05-26 10:35:46 |
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注册时间: Date of Registration: |
2026-05-26 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
急性缺血性卒中中等血管闭塞治疗策略远期预后比较:一项基于真实世界数据模拟目标试验的研究 |
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Public title: |
Long-Term Outcomes of Treatment Strategies for Acute Ischemic Stroke with Medium Vessel Occlusion: A Target Trial Emulation Study Based on Real-World Data |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
急性缺血性卒中中等血管闭塞治疗策略远期预后比较:一项基于真实世界数据模拟目标试验的研究 |
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Scientific title: |
Long-Term Outcomes of Treatment Strategies for Acute Ischemic Stroke with Medium Vessel Occlusion: A Target Trial Emulation Study Based on Real-World Data |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
黎祺 |
研究负责人: |
徐运 |
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Applicant: |
Li Qi |
Study leader: |
Xu Yun |
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申请注册联系人电话: Applicant telephone: |
+86 131 0085 8763 |
研究负责人电话:
Study leader's |
+86 139 1476 4479 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
liqiys2023@163.com |
研究负责人电子邮件: Study leader's E-mail: |
xuyun20042001@aliyun.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
江苏省南京市中山路321号 |
研究负责人通讯地址: |
江苏省南京市中山路321号 |
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Applicant address: |
No. 321, Zhongshan Road, Gulou District, Nanjing, Jiangsu, China |
Study leader's address: |
No. 321, Zhongshan Road, Gulou District, Nanjing, Jiangsu, China |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
南京鼓楼医院 |
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Applicant's institution: |
Nanjing Drum Tower Hospital |
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研究负责人所在单位: |
南京鼓楼医院 |
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Affiliation of the Leader: |
Nanjing Drum Tower Hospital |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
2025-1267-02 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
南京大学医院学附属鼓楼医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Nanjing Drum Tower Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-02-02 00:00:00 | ||
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伦理委员会联系人: |
黄季晨 |
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Contact Name of the ethic committee: |
Huang Jicheng |
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伦理委员会联系地址: |
中国江苏省南京市鼓楼区中山路321号 |
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Contact Address of the ethic committee: |
No. 321, Zhongshan Road, Gulou District, Nanjing, Jiangsu, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 25 6818 2923 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
南京鼓楼医院 |
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Primary sponsor: |
Nanjing Drum Tower Hospital |
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研究实施负责(组长)单位地址: |
中国江苏省南京市鼓楼区中山路321号 |
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Primary sponsor's address: |
No. 321, Zhongshan Road, Gulou District, Nanjing, Jiangsu, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
自选课题(自筹) |
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Source(s) of funding: |
Self-selected topic (self-funded) |
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研究疾病: |
急性缺血性卒中 |
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Target disease: |
Acute ischemic stroke |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
回顾性研究 | ||||||||||||||||||||||
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Study phase: |
Retrospective study |
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研究设计: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
1. 主要目的: 比较 EVT 与 BMT 治疗 MeVO 卒中患者的 1 年功能预后(mRS 评分)。 2. 次要目的: 评估 1 年综合预后(功能独立、生活质量、认知情绪状态);识别良好预后的预测因 素;探索 EVT 在特定亚组中的疗效。 3. 探索性目的: 分析 EVT 与长期认知功能、社会回归的相关性。 |
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Objectives of Study: |
1.Primary Objective: To compare the 1-year functional outcomes (mRS score) between EVT and BMT in patients with MeVO stroke. 2.Secondary Objectives: To assess the 1-year comprehensive outcomes (functional independence, quality of life, cognitive and emotional status); identify predictors of favorable prognosis; and explore the efficacy of EVT in specific subgroups. 3.Exploratory Objective: To analyze the correlation of EVT with long-term cognitive function and social reintegration. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1. 合并大血管闭塞; 2. 神经功能缺损症状轻微或迅速好转(接受任何治疗前); 3. 影像学提示闭塞可能为其他原因(如动脉夹层、血管炎、烟雾病); 4. 合并其他可能影响预后的颅内病变(如大的未破裂动脉瘤、动静脉畸形、颅内肿瘤); 5. 既往有严重神经系统或精神疾病,且有碍于评估神经功能; 6. 多支血管闭塞病变(例如:双侧前循环,或前后循环均闭塞); 7. 伴有预期寿命<1年的严重全身性疾病(如晚期癌症、终末期肝肾功能衰竭); 8. 预期不能完成随访。 |
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Exclusion criteria: |
1. Concurrent large vessel occlusion; 2. Mild or rapidly improving neurological deficit (prior to any treatment); 3. Imaging suggests the occlusion may be due to other causes (e.g., arterial dissection, vasculitis, moyamoya disease); 4. Presence of other intracranial pathologies that may affect prognosis (e.g., large unruptured aneurysm, arteriovenous malformation, intracranial tumor); 5. History of severe neurological or psychiatric disease that may interfere with neurological assessment; 6. Multiple vessel occlusions (e.g., bilateral anterior circulation or combined anterior and posterior circulation occlusions); 7. Severe systemic disease with a life expectancy of <1 year (e.g., advanced cancer, end-stage liver or kidney failure); 8. Inability to complete follow-up as anticipated. |
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研究实施时间: Study execute time: |
从 From 2025-12-01 00:00:00至 To 2026-12-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-02-02 00:00:00 至 To 2026-05-30 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
结束 /Completed |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
不适用 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Not applicable |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
无 |
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Blinding: |
None |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
是Yes |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
国家生物信息中心 China National center for Bioinformation (https://ngdc.cncb.ac.cn/gsub/)。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
China National center for Bioinformation (https://ngdc.cncb.ac.cn/gsub/). |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
使用电子数据采集系统(EDC),源数据来自电子病历。电子与纸质资料保存至研究结束后至少 5 年。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
An Electronic Data Capture (EDC) system is used, with the data source being electronic medical records. Both electronic and paper documents shall be preserved for at least 5 years after the completion of the study. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |