|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2500102390 |
|
最近更新日期: Date of Last Refreshed on: |
2025-05-14 08:46:46 |
|
注册时间: Date of Registration: |
2025-05-14 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
西北地区阿尔茨海默病血浆标记物的多中心临床研究 |
|
Public title: |
Study on Plasma Biomarker of Alzheimer's Disease in Northwest China |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
西北地区阿尔茨海默病血浆标记物的多中心临床研究 |
|
Scientific title: |
Study on Plasma Biomarker of Alzheimer's Disease in Northwest China |
|
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: |
高玲 |
研究负责人: |
高玲 |
|
Applicant: |
GaoLing |
Study leader: |
Ling Gao |
|
申请注册联系人电话: Applicant telephone: |
+86 15829277376 |
研究负责人电话:
Study leader's |
+86 29 85324033 |
|
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: |
linggaomed@xjtufh.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
linggaomed@xjtufh.edu.cn |
|
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: |
陕西省西安市雁塔区雁塔西路277号 |
研究负责人通讯地址: |
陕西省西安市雁塔西路277号 |
|
Applicant address: |
277 West Yanta Road, Yanta District, Xi'an, Shaanxi, China |
Study leader's address: |
277 West Yanta Road, Xi’an, Shaanxi,710061,People’s Republic of 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: |
西安交通大学第一附属医院 |
||
|
Applicant's institution: |
The First Affiliated Hospital of Xi'an Jiaotong University |
||
|
研究负责人所在单位: |
西安交通大学第一附属医院 |
||
|
Affiliation of the Leader: |
The First Affiliated Hospital of Xi'an Jiaotong University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
2025伦审医研第(423)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: |
西安交通大学第一附属医院医学伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Xian Jiaotong University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2025-03-27 00:00:00 | ||
|
伦理委员会联系人: |
易秋月 |
||
|
Contact Name of the ethic committee: |
Yi Qiuyue |
||
|
伦理委员会联系地址: |
陕西省西安市雁塔西路277号 |
||
|
Contact Address of the ethic committee: |
277 West Yanta Road, Xi’an, Shaanxi,710061,People’s Republic of China |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 29 85323473 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
yqy0118@163.com |
|
研究实施负责(组长)单位: |
西安交通大学第一附属医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The First Affiliated Hospital of Xi'an Jiaotong University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
陕西省西安市雁塔西路277号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
277 West Yanta Road, Xi’an, Shaanxi,710061,People’s Republic of China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
南京诺唯赞医疗科技有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
NanJing Vazyme Medical Technology Co.,Ltd |
||||||||||||||||||||||
|
研究疾病: |
阿尔茨海默病 |
||||||||||||||||||||||
|
Target disease: |
Alzheimer'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: |
析因分组(即根据危险因素或暴露因素分组) |
||||||||||||||||||||||
|
Study design: |
Factorial |
||||||||||||||||||||||
|
研究目的: |
1 主要目的:通过大样本、多中心的临床数据,探索血浆标志物在 AD 诊断、鉴别诊断中的价值。 2.次要目的: 1) 探讨血浆标志物在 AD 病情监测、疾病分期和预后评估中的价值; 2) 研究非 AD 痴呆患者血浆标志物的变化; 3) 探索生理因素(如年龄、性别、种族、地域)对血浆生物标志物的影响; 4) 分析血浆标志物的昼夜节律变化; 5) 其他疾病因素(如全身系统性因素、脑部疾病)对于血浆标志物的影响; 6) 分析标本保存时间及冻融状态对于血浆标志物检测的影响 |
||||||||||||||||||||||
|
Objectives of Study: |
1. Primary Objective: To explore the value of plasma biomarkers in the diagnosis and differential diagnosis of Alzheimer's disease (AD) through large-sample, multicenter clinical study. 2. Secondary Objectives: (1) To investigate the value of plasma biomarkers in disease progression monitoring, staging, and prognostic assessment of AD; (2) To study the changes of plasma biomarkers in patients with non-AD dementia; (3) To explore the impact of physiological factors (such as age, sex, race, and region) on plasma biomarkers; (4) To analyze the circadian rhythm changes of plasma biomarkers; (5) To investigate the effects of other diseases on plasma biomarkers, such as multiple chronic conditions and brain diseases; (6) To analyze the impact of sample storage time and freeze-thaw status on the detection of plasma biomarkers. |
||||||||||||||||||||||
|
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.认知障碍组纳入标准: 1) 西北地区 40 家三级、二级医院神经内科、老年科门诊及住院患者; 2) 年龄 40-85 岁(含 40 岁和 85 岁)、性别不限; 3) 明确诊断为 AD、血管性认知障碍、路易体痴呆、帕金森病痴呆、额颞 叶变性,或者其他痴呆亚型; 4) 自愿参加本研究,并签署知情同意书。 |
||||||||||||||||||||||
|
Inclusion criteria |
1.Inclusion criteria for the Cognitive Impairment Group: 1)Outpatients and inpatients from the neurology or geriatrics departments of 40 tertiary and secondary hospitals in the northwestern region of China; 2) Aged 40-85 years (including 40 and 85 years), without gender restrictions; 3.)A confirmed diagnosis of Alzheimer's disease (AD), vascular cognitive impairment, dementia with Lewy bodies, Parkinson's disease dementia, frontotemporal lobar degeneration, or other subtypes of dementia; 4) Willingness to participate in this study and signing of the informed consent form. 2. Inclusion criteria for the Non-dementia Neurological Diseases Group: 1) Outpatients and inpatients from the neurology and geriatrics departments of 40 tertiary and secondary hospitals in the northwestern region of China; 2) A confirmed diagnosis of one of the following diseases: neurodegenerative diseases (Parkinson's disease, vascular parkinsonism, multiple system atrophy, progressive supranuclear palsy, motor neuron disease), cerebrovascular diseases (acute cerebral infarction, acute spontaneous intracerebral hemorrhage, subarachnoid hemorrhage, non-acute large-area cerebral infarction), neurological immune diseases (multiple sclerosis, neuromyelitis optica spectrum disorders, myasthenia gravis), peripheral nerve diseases (Guillain-Barré syndrome), infectious encephalitis/meningitis, autoimmune encephalitis, active syphilis infection, vitamin B12 deficiency-related neurological diseases; 3) Aged 40-85 years (including 40 and 85 years), without gender restrictions; 4) Willingness to participate in this study and signing of the informed consent form. 3. Inclusion criteria for the Control Group: 1) Without definite neurological diseases; 2) From the same region as the case samples; 3) Aged 40-85 years (including 40 and 85 years), without gender restrictions; 4) Willingness to participate in this study and signing of the informed consent form. |
||||||||||||||||||||||
|
排除标准: |
1.病例组排除标准: 1) 混合型痴呆; 2) AD患者接受仑卡奈单抗治疗者; 3) 严重心、肺、肝、肾或者血液系统性疾病,或者合并肿瘤患者; 4) 拒绝抽血; 5) 拒绝签署知情同意书。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1.Exclusion criteria for the Case Group: 1. Mixed-type of dementia; 2. Patients with AD who have received lecanemab treatment; 3. Severe dysfunciton of heart, lungs, liver, kidneys, or hematological system, or patients with concurrent tumors; 4. Refused to take blood samples; 5. Refused to sign the informed consent form. 2. Exclusion criteria for the Control Group: 1) Severe dysfunciton of heart, lungs, liver, kidneys, or hematological system, or patients with concurrent tumors; 2) Refused to take blood samples; 3) Refused to sign the informed consent form. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2025-03-28 00:00:00至 To 2026-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-05-19 00:00:00 至 To 2026-12-31 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
|
||||||
|
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): |
无 |
||||||||
|
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: |
无 |
|
Blinding: |
None |
|
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): |
通过与研究负责人邮件联系提出合理诉求,待项目正式结题6月后,共享完整研究方案及结题报告中去标识化的血浆标志物检测结果,至文章出版2年止 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Contact the Principal Investigator by email to put forward reasonable demands, and we will share the complete research method and the de-identified plasma biomarker results in our final report 6 months after we formally finished our study until 2 years after publication of relevant articles. |
|
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: |
在REDCap平台进行患者病例报告表(CRF)信息录入以及数据的保存和管理。 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Patient case report form(CRF)information is entered on the REDCap platform,as well as the storage and management of data. |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |