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注册号: Registration number: |
ChiCTR2600116024 |
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最近更新日期: Date of Last Refreshed on: |
2026-01-04 17:20:58 |
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注册时间: Date of Registration: |
2026-01-04 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
基于多中心临床数据库的外周血管疾病患者长期预后及危险因素分析 |
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Public title: |
Analysis of Long-Term Outcomes and Risk Factors for Peripheral Artery Disease Using a Multi-Center Clinical Database |
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注册题目简写: |
外周血管疾病预后与危险因素的多中心数据库研究 |
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English Acronym: |
A Multicenter Database Study on Prognosis and Risk Factors in Peripheral Artery Disease |
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研究课题的正式科学名称: |
基于REDCap系统构建外周血管疾病多中心临床数据库及其应用 |
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Scientific title: |
Development and Application of a REDCap-Based Multi-Center Clinical Database for Peripheral Artery Disease |
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研究课题代号(代码): Study subject ID: |
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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: |
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申请注册联系人: |
桂亮 |
研究负责人: |
邹君杰 |
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Applicant: |
GUI Liang |
Study leader: |
ZOU Junjie |
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申请注册联系人电话: Applicant telephone: |
+86 159 5036 0001 |
研究负责人电话:
Study leader's |
+86 159 5036 0001 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
15950360001@163.com |
研究负责人电子邮件: Study leader's E-mail: |
15950360001@163.com |
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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): |
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申请注册联系人通讯地址: |
陕西省西安市雁塔西路76号 |
研究负责人通讯地址: |
江苏省南京市鼓楼区广州路300号 |
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Applicant address: |
76 Yanta West Road, Yanta District, Xi'an, Shaanxi Province, China |
Study leader's address: |
300 Guangzhou Road, Gulou District, Nanjing, Jiangsu Province, China |
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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: |
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申请人所在单位: |
西安交通大学公共卫生学院 |
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Applicant's institution: |
School of Public Health, Xi’an Jiaotong University |
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研究负责人所在单位: |
南京医科大学第一附属医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Nanjing Medical University |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
2023-SR-471 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
南京医科大学第一附属医院(江苏省人民医院)伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of The First Affiliated Hospital of Nanjing Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-08-08 00:00:00 | ||
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伦理委员会联系人: |
025-68306360 |
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Contact Name of the ethic committee: |
+86-25-68306360 |
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伦理委员会联系地址: |
南京市广州路300号江苏省人民医院7号楼3楼 |
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Contact Address of the ethic committee: |
3rd Floor, Building 7, Jiangsu Province Hospital, 300 Guangzhou Road, Nanjing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 25 6830 6360 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
西安交通大学公共卫生学院 |
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Primary sponsor: |
School of Public Health, Xi’an Jiaotong University |
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研究实施负责(组长)单位地址: |
陕西省西安市雁塔西路76号 |
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Primary sponsor's address: |
76 Yanta West Road, Yanta District, Xi'an, Shaanxi Province, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
本研究为研究者发起的研究(IIT),无外部资助。经费由南京医科大学第一附属医院自筹。REDCap数据平台由西安交通大学公共卫生学院提供支持,生物样本检测由南京医科大学第一附属医院公共实验中心完成 |
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Source(s) of funding: |
This is an investigator-initiated trial (IIT) with no external funding. The study is self-funded by The First Affiliated Hospital of Nanjing Medical University. The REDCap data platform is supported by the School of Public Health, Xi’an Jiaotong University, and biospecimen testing is conducted by the hospital‘s Public Experiment Center. |
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研究疾病: |
外周动脉疾病 |
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Target disease: |
Peripheral Arterial Disease |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
通过基于REDCap系统构建外周动脉疾病多中心临床数据库并运用,有效转化的多中心、高质量临床研究数据,为外周动脉疾病的防治提供新的方向。 |
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Objectives of Study: |
To establish and utilize a multi-center clinical database for peripheral arterial disease based on the REDCap system, thereby transforming and applying high-quality, multi-center clinical research data to provide new directions for the prevention and treatment of peripheral arterial disease. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1.合并有严重心脑血管、肺、肝、肾和造血系统严重原发疾病及精神病者 2.并发炎症、肿瘤性疾病 3.近三个月内已参加与本试验有干扰的药物或其他医疗器械临床试验者 4.过敏体质及相关药物过敏者 5.妊娠和哺乳期的妇女 6.不能或不同意参与本试验者 |
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Exclusion criteria: |
1.Patients with severe primary diseases of the cardiovascular, cerebrovascular, pulmonary, hepatic, renal, or hematopoietic systems, or psychiatric disorders. 2.Patients with concurrent inflammatory or neoplastic diseases. 3.Patients who have participated in other drug or medical device clinical trials that may interfere with this trial within the past three months. 4.Patients with allergic constitution or relevant drug allergies. 5.Women who are pregnant or breastfeeding. 6.Patients who are unable or unwilling to participate in this trial. |
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研究实施时间: Study execute time: |
从 From 2025-12-12 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-01-10 00:00:00 至 To 2027-12-31 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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 |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
否No |
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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): |
本研究的原始病例数据(包含个人可识别信息)将在研究完成后按规定进行销毁,因此不提供原始数据共享。经完全去标识化处理的统计分析结果将通过学术期刊发表。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The original case record data (containing personally identifiable information) from this study will be destroyed upon study completion in accordance with established protocols and therefore will not be available for sharing. Fully de-identified statistical analysis results will be disseminated through publication in academic journals. |
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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: |
本研究采用电子化数据采集与管理。数据通过设计好的电子病例报告表(eCRF)进行收集。所有数据将通过基于互联网的电子数据采集(EDC)系统——REDCap(Research Electronic Data Capture)进行录入和管理。该REDCap系统由本研究的组长单位(西安交通大学公共卫生学院)提供并负责维护,确保数据安全与多中心协同工作。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
This study employs electronic data capture and management. Data is collected using designed electronic Case Report Forms (eCRFs). All data will be entered and managed via an internet-based Electronic Data Capture (EDC) system—REDCap (Research Electronic Data Capture). This REDCap system is provided and maintained by the leading unit of this study (School of Public Health, Xi’an Jiaotong University), ensuring data security and multi-center collaboration. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |