ChiCTR2000032012 版本V1.3 版本创建时间2020/04/17 19:12:37 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2000032012 

最近更新日期:

Date of Last Refreshed on:

2020-04-17 19:08:18 

注册时间:

Date of Registration:

2020-04-17 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

区分衰弱亚型的神经影像学标志物

Public title:

Neuroimaging Biomarkers of Frailty

注册题目简写:

English Acronym:

研究课题的正式科学名称:

区分衰弱亚型的神经影像学标志物

Scientific title:

Neuroimaging Biomarkers of Frailty

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:

史慧 

研究负责人:

夏鑫/薛千里 

Applicant:

Hui Shi 

Study leader:

Xin Xia/ Qian-Li Xue 

申请注册联系人电话:

Applicant telephone:

+86 15832195395

研究负责人电话:

Study leader's telephone:

+86 18736040958

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:

hui_s27@163.com

研究负责人电子邮件:

Study leader's E-mail:

a_siasin@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:

四川省成都市武侯区国学巷37号

研究负责人通讯地址:

四川省成都市武侯区国学巷37号

Applicant address:

37 Guoxue Lane, Chengdu, Sichuan, China

Study leader's address:

37 Guoxue Lane, Chengdu, Sichuan, China

申请注册联系人邮政编码:

Applicant postcode:

610041

研究负责人邮政编码:

Study leader's postcode:

610041

申请人所在单位:

四川大学华西医院

Applicant's institution:

West China Hospital, Sichuan University

研究负责人所在单位:

四川大学华西医院

Affiliation of the Leader:

West China Hospital, Sichuan University

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2019年 审(979)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:

四川大学华西医院临床试验伦理委员会

Name of the ethic committee:

Clinical Trial Ethics Committee, West China Hospital of Sichuan University

伦理委员会批准日期:

Date of approved by ethic committee:

2020-01-08 00:00:00

伦理委员会联系人:

李娜、庞昭

Contact Name of the ethic committee:

Na Li, Pang Zhao

伦理委员会联系地址:

四川省成都市武侯区国学巷37号四川大学华西医院老八教412-413室

Contact Address of the ethic committee:

Room 412-413, Old 8th Teaching Building, West China Hospital, Sichuan University, 37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 028-85422654

伦理委员会联系人邮箱:

Contact email of the ethic committee:

huaxilunli@163.com

研究实施负责(组长)单位:

四川大学华西医院

Primary sponsor:

West China Hospital, Sichuan University

研究实施负责(组长)单位地址:

四川省成都市武侯区国学巷37号

Primary sponsor's address:

37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

经费或物资来源:

四川大学华西医院

Source(s) of funding:

West China Hospital of Sichuan University

Target disease:

senile disease

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)通过对大脑进行神经影像学方面的研究,以评估颅脑结构、 功能以及淀粉样蛋白的沉积变化。 (2)通过鉴别神经影像标志物,区分四类患者“无生理衰弱,无认知功能障碍”,“单纯的生理衰弱”,“单纯认知功能障碍”和“生理衰弱合并认知功能障碍”。 (3)“生理衰弱合并认知功能障碍”表型与血管的神经影像学标志物之间的关联,以及合并表型与神经退行病性之间的病因学关联。  

Objectives of Study:

(1) To conduct neuroimaging study of the brain to assess integrity of brain structure, function, and amyloid deposit; (2) To identify neuroimaging markers that distinguish patients with neither frailty nor cognitive impairment from those with frailty alone, or cognitive impairment alone, or both frailty and cognitive impairment; (3) To assess the associations between the combined phenotype as defined in Aim (2) and neuroimaging evidence of vascular vs. neurodegenerative pathologies.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1)性别(男/女);
2)年龄≥65岁;
3)签署知情同意并能遵循实验研究流程;

Inclusion criteria

1. both genders;
2. aged ≥60 years;
3. capacity to give informed consent and follow study procedures.

排除标准:

1)已确诊患有危及生命的严重疾病,其预期寿命小于6个月;
2)严重的视觉或听觉障碍,可能干扰认知功能和生理衰弱评估的完成;
3) MRI 扫描禁忌症患者:幽闭症患者、带有金属材料、不兼容心脏起搏器的携带者、内部除颤器或带有其他铁磁体植入物,无法配合完成神经影像学检查者;
4)患有严重认知障碍的患者(MoCA<6 或不可测试);
5)患有严重心理精神疾病患者:如严重抑郁症(PHQ-8>20);
6) 患严重心脏功能障碍:如急性失代偿性心力衰竭和/或慢性心力衰竭功能III或IV期(纽约心脏学会分类法);
7) 患严重肺功能障碍:慢性阻塞性肺病III或IV期(GOLD分类)的急性恶化,和/或氧分压(PaO2)水平<60 mmHg;
8)帕金森病史;
9)头部创伤或昏厥史;
10)正在使用安眠药、止痛药(包括阿司匹林)或其他已知影响大脑功能的制剂(例如,抗组胺药、减(轻)充血剂,多奈哌齐、银杏制剂等等)。

Exclusion criteria:

1) known diagnosis of severe disease that are life-threatening with expected life expectancy of less than six months;
2) severe visual or auditory deficits that may interfere with the completion of cognitive function and physical frailty assessments;
3) patients with contraindications for the MRI and PET scan: claustrophobia, metallic materials, carriers of non-compatible pacemaker, internal defibrillator or other ferromagnetic implants not allowing going to the service of neuroimaging;
4) patients with severe cognitive impairment (MoCA <6 or not testable);
5) patients with severe psychiatric illness: such as severe depression (PHQ-8 >20);
6) severe cardiac dysfunction: acute decompensated heart failure and/or chronic heart failure functional class III or IV (New York Heart Association classification);
7) severe pulmonary dysfunction: acute exacerbation of chronic obstructive lung disease stage III or IV (GOLD classification), and/or PaO2 levels < 60 mmHg;
8) history of Parkinson's;
9) a history of head trauma or fainting;
10) currently using sleeping aids, painkillers (including aspirin), or other agents known to affect brain function (for instance, antihistamines, decongestants, et c).

研究实施时间:

Study execute time:

From 2020-01-01 00:00:00 To 2021-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-05-01 00:00:00 To 2021-12-31 00:00:00  

干预措施:

Interventions:

组别:

Case series

样本量:

100

Group:

Case series

Sample size:

干预措施:

干预措施代码:

Intervention:

Nil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

四川 

市(区县):

成都 

Country:

China 

Province:

SIchuan 

City:

Chengdu 

单位(医院):

四川大学华西医院 

单位级别:

三甲医院 

Institution
hospital:

West China Hospital, Sichuan University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

磁共振数据

指标类型:

主要指标

Outcome:

Magnetic Resonance Imaging

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

生理衰弱

指标类型:

主要指标

Outcome:

physical frailty

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

衰弱相关炎性标志物

指标类型:

次要指标

Outcome:

frailty biomarkers

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

认知功能

指标类型:

附加指标

Outcome:

cognitive function

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:

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 65 years
最大 Max age 100 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):

不适用

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

N/A

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

N/A

Blinding:

N/A

是否共享原始数据:

IPD sharing

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):

不公开

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

Private

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:

病例记录表

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

Case Record Form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2020-04-17 19:05:06