住院脑小血管病人群的队列研究

注册号:

Registration number:

ChiCTR2200058443 

最近更新日期:

Date of Last Refreshed on:

2024-01-08 02:12:38 

注册时间:

Date of Registration:

2022-04-09 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

住院脑小血管病人群的队列研究

Public title:

Cohort study of Inpatients with Cerebral Small Vessel Disease

注册题目简写:

English Acronym:

研究课题的正式科学名称:

住院脑小血管病人群的队列研究

Scientific title:

Cohort study of Inpatients with Cerebral Small Vessel Disease

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:

朱文浩 

研究负责人:

朱文浩 

Applicant:

Wenhao Zhu 

Study leader:

Wenhao Zhu 

申请注册联系人电话:

Applicant telephone:

+86 13437196982

研究负责人电话:

Study leader's
telephone:

+86 13437196982

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:

tianyalinghu@126.com

研究负责人电子邮件:

Study leader's E-mail:

tianyalinghu@126.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:

湖北省武汉市硚口区解放大道1095号

研究负责人通讯地址:

湖北省武汉市硚口区解放大道1095号

Applicant address:

1095 Jiefang Avenue, Qiaokou District, Wuhan, Hubei

Study leader's address:

1095 Jiefang Avenue, Qiaokou District, Wuhan, Hubei

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:

华中科技大学同济医学院附属同济医院

Applicant's institution:

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

研究负责人所在单位:

华中科技大学同济医学院附属同济医院

Affiliation of the Leader:

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

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:

TJ-IRB20210731

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:

华中科技大学同济医学院附属同济医院医学伦理委员会

Name of the ethic committee:

The Medical Ethics Committee of Tongji Hospital, Tongji Medical Colledge, Huazhong University of Science and Technology

伦理委员会批准日期:

Date of approved by ethic committee:

2021-07-28 00:00:00

伦理委员会联系人:

杜艾桦

Contact Name of the ethic committee:

Aihua Du

伦理委员会联系地址:

湖北省武汉市硚口区解放大道1095号

Contact Address of the ethic committee:

1095 Jiefang Avenue, Qiaokou District, Wuhan, Hubei

伦理委员会联系人电话:

Contact phone of the ethic committee:

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:

华中科技大学同济医院附属同济医院

Primary sponsor:

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

研究实施负责(组长)单位地址:

湖北省武汉市解放大道1095号

Primary sponsor's address:

1095 Jiefang Avenue, Qiaokou District, Wuhan, Hubei

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

湖北

市(区县):

武汉

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

华中科技大学同济医学院附属同济医院

具体地址:

湖北省武汉市解放大道1095号

Institution
hospital:

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Address:

1095 Jiefang Avenue, Qiaokou District, Wuhan, Hubei

经费或物资来源:

国家自然科学基金(81801146)、湖北省自然科学基金(2021CFB382)、湖北省重点研发计划(2020BCA070)、武汉市应用基础前沿项目(2020020601012226)、武汉市应急科技攻关专项项目(2020020401010096)、同济医院临床研究领航项目(2019CR106)

Source(s) of funding:

The National Natural Science Foundation of China (No.81801146), the Natural Science Foundation of Hubei Province (No.2021CFB382), the Key R & D program of Hubei Province (No. 2020BCA070)

研究疾病:

脑小血管病  

Target disease:

Cerebral small vessel disease

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:

1. 明确CSVD人群的临床和影像学转归特点,发现新的CSVD危险因素; 2. 深入探讨CSVD临床和影像学转归背后的机制,以及二者之间的联系; 3. 基于人工智能技术,建立CSVD的精准分型系统,以及CSVD的认知障碍、疲劳、情感障碍和影像学改变等多维度预测模型。  

Objectives of Study:

1. To identify the clinical and imaging characteristics of CSVD and find new risk factors of CSVD; 2. To explore the mechanisms underlying the clinical and imaging conversion of CSVD and the relationship between them; 3. To establish an accurate classification system and multi-dimensional prediction models of cognitive impairment, fatigue, affective disorders and imaging changes in CSVD based on artificial intelligence technology.

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. 独立生活能力明显受限,无法配合完成检查;
2. 目前有脑出血,蛛网膜下腔出血,颅内占位性病变等疾病;
3. 基线时有梗死灶大于2cm的急性缺血性脑卒中或严重卒中(NIHSS评分≧15分);
4. 合并有重度抑郁焦虑症影响依从性和可靠性;
5. 合并有精神分裂症等严重的精神障碍;
6. 存在引起脑白质病变的其他非血管源性疾病,包括CO中毒,重金属中毒,多发性硬化,肾上腺脑白质营养不良等;
7. 存在其他非血管性原因所致痴呆或认知损害(如额颞叶痴呆,阿尔茨海默病,路易体痴呆,朊蛋白病,帕金森病,自身免疫性脑炎等);
8. 存在严重的全身性疾患,如严重的肝肾疾病、呼吸系统疾病、恶性肿瘤者;严重的急性感染者;
9. 有明显的听力或视力受损、语言障碍,幽闭恐惧症等导致患者不能配合神经心理量表评估和MRI检查;
10. 预计寿命小于3年者;
11. 研究期间不能按要求随访的患者。

Exclusion criteria:

1. Significantly limited independent living ability, and unable to cooperate to complete the inspection;
2. Cerebral hemorrhage, subarachnoid hemorrhage, intracranial space-occupying lesions and other diseases at present;
3. Acute ischemic stroke with infarction diameter greater than 2cm, or severe stroke at baseline (NIHSS score ≥ 15);
4. Severe depression and anxiety;
5. Serious mental disorders such as schizophrenia;
6. Other nonvascular diseases that cause leukoencephalopathy, including CO poisoning, multiple sclerosis and adrenoleukodystrophy;
7. Dementia or cognitive impairment caused by other non vascular causes (such as frontotemporal dementia, Alzheimer's disease, Lewy body dementia, prion protein disease, Parkinson's disease, autoimmune encephalitis, etc.);
8. Serious systemic diseases, such as serious liver and kidney diseases, respiratory diseases, cancer, and severe acute infection;
9. Subjects who can not cooperate with neuropsychological assessment and MRI examination due to obvious hearing or vision impairment, language disorder, claustrophobia, etc.;
10. The expected service life is less than 1 year;
11. Patients who could not be followed up during the study.

研究实施时间:

Study execute time:

From 2022-04-20 00:00:00 To 2024-04-20 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-04-20 00:00:00 To 2027-04-20 00:00:00

干预措施:

Interventions:

组别:

样本量:

Group:

Sample size:

干预措施:

干预措施代码:

Intervention:

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖北 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

华中科技大学同济医学院附属同济医院 

单位级别:

三甲 

Institution
hospital:

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

人口统计学资料

指标类型:

主要指标

Outcome:

Demographic data

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

既往史及危险因素

指标类型:

主要指标

Outcome:

Past history and risk factors

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

家族史

指标类型:

主要指标

Outcome:

Family history

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

影像学资料

指标类型:

主要指标

Outcome:

Imaging data

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

日常生活能力评估

指标类型:

主要指标

Outcome:

Assessment of daily living ability

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

总体认知测试及痴呆评估

指标类型:

主要指标

Outcome:

Overall Cognitive Test and Dementia Assessment

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

新发卒中

指标类型:

主要指标

Outcome:

New stroke

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

新发心血管事件

指标类型:

主要指标

Outcome:

New cardiovascular events

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

分领域认知测试

指标类型:

主要指标

Outcome:

Subdomain Cognitive Test

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

总体健康状况评估

指标类型:

主要指标

Outcome:

General health assessment

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

疲劳评定

指标类型:

主要指标

Outcome:

Fatigue assessment

Type:

Primary 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:

尿液

组织:

Sample Name:

Urine

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

粪便

组织:

Sample Name:

Stool

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

血液

组织:

Sample Name:

Blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

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):

本研究未涉及随机化分组

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

Randomized grouping was not involved in this study.

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):

2027年6月,通过中国临床试验注册中心官网公布, 网址:http://www.chictr.org.cn/usercenter.aspx

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

Data will be shared in June 2027,through China clinical trial registry, URL:http://www.chictr.org.cn/usercenter.aspx

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:

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)

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

Data acquisition and management consists of two parts, one is Case Record Form (CRF), the other is Electronic Data Capture and management system (EDC).

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-04-09 20:26:25