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

注册号:

Registration number:

ChiCTR2600126479 

最近更新日期:

Date of Last Refreshed on:

2026-06-09 17:38:17 

注册时间:

Date of Registration:

2026-06-09 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

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

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

注册题目简写:

STAR-TNK Ⅱ

English Acronym:

STAR-TNK II

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

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

研究课题代号(代码):

Study subject ID:

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:

申请注册联系人:

王自然 

研究负责人:

王自然 

Applicant:

ZiRan Wang 

Study leader:

ZiRan Wang 

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
telephone:

+86 139 5499 3801

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

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

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):

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

Applicant address:

27 Jiefang Road East, Lanshan District, Linyi,Shandong, China

Study leader's address:

27 Jiefang Road East, Lanshan District, Linyi,Shandong, China

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:

申请人所在单位:

临沂市人民医院

Applicant's institution:

Linyi People's Hospital

研究负责人所在单位:

临沂市人民医院

Affiliation of the Leader:

Linyi People's Hospital

是否获伦理委员会批准:

Approved by ethic committee:

Yes

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

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

Name of the ethic committee:

Science and Technology Ethics Committee, Linyi People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2026-03-16 00:00:00

伦理委员会联系人:

尹甲伟

Contact Name of the ethic committee:

Jiawei Yin

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

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

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:

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)

Primary sponsor:

Linyi People's Hospital (Shandong Provincial Clinical Research Center for Geriatric Diseases)

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

Primary sponsor's address:

27 Jiefang Road East, Lanshan District, Linyi, Shandong, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

山东

市(区县):

临沂

Country:

China

Province:

Shandong

City:

Linyi

单位(医院):

临沂市人民医院

具体地址:

中国山东省临沂市兰山区解放路东段27号

Institution
hospital:

Linyi People's Hospital

Address:

27 Jiefang Road East, Lanshan District, Linyi, Shandong, China

经费或物资来源:

单位自筹

Source(s) of funding:

Self raised funds by the unit

研究疾病:

急性缺血性卒中  

Target disease:

Acute ischemic stroke

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

队列研究 

Study design:

Cohort study 

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。  

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.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

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。

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.

研究实施时间:

Study execute time:

From 2026-03-15 00:00:00 To 2028-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2026-06-10 00:00:00 To 2027-12-31 00:00:00

干预措施:

Interventions:

组别:

病例组

样本量:

20000

Group:

Case series

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

山东 

市(区县):

临沂 

Country:

China

Province:

Shandong

City:

Linyi

单位(医院):

临沂市人民医院 

单位级别:

三甲 

Institution
hospital:

Linyi People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

静脉溶栓治疗后36 小时内症状性颅内出血(按照ECASSIII定义)

指标类型:

主要指标

Outcome:

Symptomatic intracranial hemorrhage within 36 hours after intravenous thrombolysis (according to the ECASS III definition)

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

90 天时良好功能预后(mRS 评分≤1分)

指标类型:

主要指标

Outcome:

Good functional prognosis at 90 days (mRS score ≤1)

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

90 天时功能独立(mRS 评分≤2 分)

指标类型:

次要指标

Outcome:

Functional independence at 90 days (mRS score ≤2)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

90 天时有序mRS 评分

指标类型:

次要指标

Outcome:

90-day ordinal mRS score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

24hNIHSS 相对于基线的变化(短期功能预后)

指标类型:

次要指标

Outcome:

Change in 24h NIHSS relative to baseline (short-term functional prognosis)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

7 天/出院 NIHSS 相对于基线的变化(短期功能预后)

指标类型:

次要指标

Outcome:

Change in 7-day/discharge NIHSS relative to baseline (short-term functional prognosis)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

90 天内全因死亡及死亡时间

指标类型:

次要指标

Outcome:

All-cause mortality and time of death within 90 days

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

90 天内卒中复发及复发时间

指标类型:

次要指标

Outcome:

Stroke recurrence and recurrence time within 90 days

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

住院期间严重不良事件

指标类型:

次要指标

Outcome:

Serious adverse events during hospitalization

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

到院至开始静脉溶栓时间(DNT)

指标类型:

附加指标

Outcome:

Door-to-Needle Time (DNT)

Type:

Additional indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

None

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

Randomization Procedure (please state who generates the random number sequence and by what method):

None

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

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

是Yes

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):

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

None

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

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2026-06-09 17:37:42