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注册号: Registration number: |
ChiCTR2600126479 |
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最近更新日期: Date of Last Refreshed on: |
2026-06-09 17:38:17 |
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注册时间: Date of Registration: |
2026-06-09 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
急性缺血性卒中再灌注治疗-替奈普酶 (rhTNK-tPA,明复乐)静脉溶栓真实世界数据监测登记研究 |
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Public title: |
Acute Ischemic Stroke Reperfusion Therapy - Recombinant Human TNK Tissue-type Plasminogen Activator for Injection (rhTNK-tPA, Mingfule) Real-World Data Monitoring Registry Study for Intravenous Thrombolysis |
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注册题目简写: |
STAR-TNK Ⅱ |
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English Acronym: |
STAR-TNK II |
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研究课题的正式科学名称: |
急性缺血性卒中再灌注治疗-替奈普酶 (rhTNK-tPA,明复乐)静脉溶栓真实世界数据监测登记研究 |
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Scientific title: |
Acute Ischemic Stroke Reperfusion Therapy - Recombinant Human TNK Tissue-type Plasminogen Activator for Injection (rhTNK-tPA, Mingfule) Real-World Data Monitoring Registry Study for Intravenous Thrombolysis |
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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: |
王自然 |
研究负责人: |
王自然 |
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Applicant: |
ZiRan Wang |
Study leader: |
ZiRan Wang |
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申请注册联系人电话: Applicant telephone: |
+86 139 5499 3801 |
研究负责人电话:
Study leader's |
+86 139 5499 3801 |
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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: |
wzr0806@163.com |
研究负责人电子邮件: Study leader's E-mail: |
wzr0806@163.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: |
中国山东省临沂市兰山区解放路东段27号 |
研究负责人通讯地址: |
中国山东省临沂市兰山区解放路东段27号 |
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Applicant address: |
27 Jiefang Road East, Lanshan District, Linyi,Shandong, China |
Study leader's address: |
27 Jiefang Road East, Lanshan District, Linyi,Shandong, 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: |
临沂市人民医院 |
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Applicant's institution: |
Linyi People's Hospital |
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研究负责人所在单位: |
临沂市人民医院 |
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Affiliation of the Leader: |
Linyi People's 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: |
科技伦审第(202603-H-033)号 |
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: |
临沂市人民医院科技伦理委员会 |
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Name of the ethic committee: |
Science and Technology Ethics Committee, Linyi People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2026-03-16 00:00:00 | ||
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伦理委员会联系人: |
尹甲伟 |
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Contact Name of the ethic committee: |
Jiawei Yin |
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伦理委员会联系地址: |
中国山东省临沂市北城新区临沂市人民医院北城院区12号楼715室 |
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Contact Address of the ethic committee: |
Room 715, Building 12, North Campus of Linyi People's Hospital, North New District of Linyi City, Shandong Province, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 183 1549 0257 |
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: |
临沂市人民医院(山东省老年疾病临床医学研究中心) |
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Primary sponsor: |
Linyi People's Hospital (Shandong Provincial Clinical Research Center for Geriatric Diseases) |
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研究实施负责(组长)单位地址: |
中国山东省临沂市兰山区解放路东段27号 |
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Primary sponsor's address: |
27 Jiefang Road East, Lanshan District, Linyi, Shandong, 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: |
单位自筹 |
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Source(s) of funding: |
Self raised funds by the unit |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
通过前瞻性、多中心、连续登记的真实世界研究,监测急性缺血性卒中患者在接受替奈普酶(rhTNK-tPA,明复乐)静脉溶栓治疗后各个层面的有效性及安全性。 |
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Objectives of Study: |
Through a prospective, multicenter, continuous registry real-world study, monitor the effectiveness and safety of acute ischemic stroke patients at all levels after receiving intravenous thrombolytic therapy with rhTNK-tPA. |
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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. 院外已经接受再灌注治疗的患者(如入院前已静脉溶栓的患者); 2. 参与其他临床试验并且可能影响本研究结果的患者。 |
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Exclusion criteria: |
1. Patients who have already received reperfusion therapy outside the hospital (such as patients who have received intravenous thrombolysis before admission); 2. Patients participating in other clinical trials that may affect the results of this study. |
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研究实施时间: Study execute time: |
从 From 2026-03-15 00:00:00至 To 2028-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-06-10 00:00:00 至 To 2027-12-31 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: |
尚未开始 Not yet recruiting |
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): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
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Blinding: |
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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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |