ChiCTR2500102965 版本V1.0 版本创建时间2025/05/22 10:30:51 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:

ChiCTR2500102965 

最近更新日期:

Date of Last Refreshed on:

2025-05-22 10:30:24 

注册时间:

Date of Registration:

2025-05-22 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

血脑屏障破坏参与伴2型糖尿病的帕金森病患者的认知损害

Public title:

Blood-brain barrier disruption is involved in cognitive impairment of Parkinson's disease patients with type 2 diabetes

注册题目简写:

English Acronym:

研究课题的正式科学名称:

血脑屏障功能障碍在伴2型糖尿病的帕金森病患者认知障碍中的作用研究

Scientific title:

Invovlement of blood-brain barrier dysfunction in cognitive impairment of Parkinson's disease patients with type 2 diabetes

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:

卢节平 

研究负责人:

卢节平 

Applicant:

Jieping Lu 

Study leader:

Jieping Lu 

申请注册联系人电话:

Applicant telephone:

+86 151 5516 8226

研究负责人电话:

Study leader's
telephone:

+86 551 62284084

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:

lujp@ustc.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

lujp1984@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:

安徽合肥市庐江路17号

研究负责人通讯地址:

安徽省合肥市庐江路17号

Applicant address:

No. 17, Lujiang Road, Hefei City, Anhui Province

Study leader's address:

No. 17, Lujiang Road, Hefei City, Anhui Province

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:

中国科学技术大学附属第一医院

Applicant's institution:

The First Affiliated Hospital of University of Science and Technology of China

研究负责人所在单位:

中国科学技术大学附属第一医院(安徽省立医院)

Affiliation of the Leader:

The First Affiliated Hospital of University of Science and Technology of China

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:

2024KY伦审第542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:

中国科学技术大学附属第一医院医学研究伦理委员会

Name of the ethic committee:

Medical Research Ethics Committee of The First Affiliated Hospital of USTC

伦理委员会批准日期:

Date of approved by ethic committee:

2024-11-27 00:00:00

伦理委员会联系人:

胡怡然

Contact Name of the ethic committee:

Hu YiRan

伦理委员会联系地址:

安徽省合肥市庐江路17号

Contact Address of the ethic committee:

No. 17, Lujiang Road, Hefei City, Anhui Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 551 62282931

伦理委员会联系人邮箱:

Contact email of the ethic committee:

isabel0125@126.com

研究实施负责(组长)单位:

中国科学技术大学附属第一医院(安徽省立医院)

Primary sponsor:

The First Affiliated Hospital of University of Science and Technology of China

研究实施负责(组长)单位地址:

安徽省合肥市庐江路17号

Primary sponsor's address:

No. 17, Lujiang Road, Hefei City, Anhui Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

安徽

市(区县):

Country:

China

Province:

Anhui

City:

单位(医院):

中国科学技术大学附属第一医院(安徽省立医院)

具体地址:

安徽省合肥市庐江路17号

Institution
hospital:

The First Affiliated Hospital of University of Science and Technology of China

Address:

No. 17, Lujiang Road, Hefei City, Anhui Province

经费或物资来源:

中央高校基本科研业务费专项资金

Source(s) of funding:

Fundamental Research Funds for the Central Universities

研究疾病:

帕金森病  

Target disease:

Parkinson's 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:

病例对照研究 

Study design:

Case-Control study 

研究目的:

探究伴T2DM的PD患者是否存在更严重的BBB功能障碍以及其认知障碍是否与特定脑区BBB渗漏以及脑区脑结构改变有关。  

Objectives of Study:

To explore whether PD patients with T2DM have more severe BBB dysfunction,and whether their cognitive impairment is related to BBB leakage and brain structure changes in specific brain areas.

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) 伴发T2DM或不伴T2DM的PD患者;
2) 年龄18-80周岁(含),性别不限;

Inclusion criteria

1)?Parkinson's disease patients with?or?without?T2DM;
2) No gender limitation, age 18-80 (including 18 and 80 years old);

排除标准:

1)有痴呆史;
2)有精神病史或正在接受精神疾病治疗,如服用抗焦虑药、抗抑郁药、情绪稳定剂、抗精神病药及其他可能干扰评估的药物;
3)有药物滥用或依赖史;
4)孕妇;
5)可能影响评估的严重身体疾病;
6)MRI扫描禁忌;
7)拒绝参与;

Exclusion criteria:

1) a history of dementia;
2) a history of mental disorders or current treatment for mental illnesses, such as taking anxiolytics, antidepressants, mood stabilizers, antipsychotics and other drugs that may interfere with the assessment;
3) a history of drug abuse or dependence;
4) pregnant women;
5) severe physical illnesses that may interfere with the assessment;
6) contraindication to MRI scan;
7) declining to participate.

研究实施时间:

Study execute time:

From 2024-12-20 00:00:00 To 2027-07-15 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-06-05 00:00:00 To 2026-03-31 00:00:00

干预措施:

Interventions:

组别:

伴 T2DM 的 PD 组

样本量:

30

Group:

PD group with T2DM

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

不伴 T2DM 的 PD 组

样本量:

30

Group:

PD group without T2DM

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):

安徽 

市(区县):

 

Country:

China

Province:

Anhui

City:

单位(医院):

中国科学技术大学附属第一医院(安徽省立医院) 

单位级别:

三级甲等 

Institution
hospital:

The First Affiliated Hospital of University of Science and Technology of China

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

PD-CRS量表得分

指标类型:

主要指标

Outcome:

PD-CRS scores

Type:

Primary indicator

测量时间点:

入组时

测量方法:

量表评估

Measure time point of outcome:

At the time of enrollment

Measure method:

scale assessment

指标中文名:

不同脑区Ktrans值和Vp值

指标类型:

主要指标

Outcome:

Ktrans values and Vp values in different brain regions

Type:

Primary indicator

测量时间点:

入组时

测量方法:

SPM12和BRANT软件

Measure time point of outcome:

At the time of enrollment

Measure method:

SPM12 and BRANT

指标中文名:

特定脑区容积和皮层厚度

指标类型:

主要指标

Outcome:

The volumes of specific brain regions and cortical thickness

Type:

Primary indicator

测量时间点:

入组时

测量方法:

MRI机器自带软件

Measure time point of outcome:

At the time of enrollment

Measure method:

the software of the MRI machine

指标中文名:

血清可溶性ICAM-1、VCAM-1和S100B蛋白含量

指标类型:

次要指标

Outcome:

Serum levels of soluble ICAM-1、VCAM-1 and S100B

Type:

Secondary indicator

测量时间点:

入组时

测量方法:

ELISA

Measure time point of outcome:

At the time of enrollment

Measure method:

ELISA

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 18 years
最大 Max age 80 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:

不公开/Private

盲法:

Blinding:

None

是否共享原始数据:

IPD sharing

否No

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:

病例观察表和电子资料由本课题研究人员进行采集、管理和保存

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

The case record form and electronic data will be recorded and kept by special research assistants

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2025-05-22 10:30:24