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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2400079516 |
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最近更新日期: Date of Last Refreshed on: |
2024-01-05 08:59:15 |
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注册时间: Date of Registration: |
2024-01-05 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: |
钠-葡萄糖协同转运蛋白 2 抑制剂治疗未合并糖尿病的慢性肾脏病患者的肾脏保护有效性和安全性的真实世界研究方案 |
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Public title: |
A real-world study of the renoprotective efficacy and safety of sodium-glucose co-transporter protein 2 inhibitors in the treatment of Chronic kidney disease patients without diabetes mellitus |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
钠-葡萄糖协同转运蛋白 2 抑制剂治疗未合并糖尿病的慢性肾脏病患者的肾脏保护有效性和安全性的真实世界研究方案 |
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Scientific title: |
A real-world study of the renoprotective efficacy and safety of sodium-glucose co-transporter protein 2 inhibitors in the treatment of Chronic kidney disease patients without diabetes mellitus |
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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: |
刘珂 |
研究负责人: |
刘芳 |
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Applicant: |
Ke Liu |
Study leader: |
Fang Liu |
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申请注册联系人电话: Applicant telephone: |
+86 188 7521 6408 |
研究负责人电话: Study leader's telephone: |
+86 189 8060 1214 |
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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: |
lk02022@163.com |
研究负责人电子邮件: Study leader's E-mail: |
liufangfh@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: |
中国四川省成都市国学巷37号 |
研究负责人通讯地址: |
中国四川省成都市国学巷37号 |
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Applicant address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
Study leader's address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, 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: |
四川大学华西医院肾脏科 |
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Applicant's institution: |
Division of Nephrology, West China Hospital of Sichuan University |
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研究负责人所在单位: |
四川大学华西医院肾脏科 |
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Affiliation of the Leader: |
Division of Nephrology, West China Hospital of Sichuan University |
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是否获伦理委员会批准: |
是/Yes |
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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年审(2008)号 |
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: |
四川大学华西医院医学伦理审查委员会 |
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Name of the ethic committee: |
Clinical Trial Ethics Committee of West China Hospital, Sichuan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-11-13 00:00:00 |
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伦理委员会联系人: |
邓邵林 |
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Contact Name of the ethic committee: |
Shaolin Deng |
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伦理委员会联系地址: |
中国四川省成都市国学巷37号 |
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Contact Address of the ethic committee: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 8542 3237 |
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: |
四川大学华西医院 |
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Primary sponsor: |
West China Hospital, Sichuan University |
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研究实施负责(组长)单位地址: |
四川省成都市国学巷37号 |
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Primary sponsor's address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, 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: |
四川省卫生健康委员会 |
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Source(s) of funding: |
Health commission of Sichuan province |
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Target disease: |
Chronic kidney disease without diabetes mellitus |
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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: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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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: |
研究旨在用真实世界的数据,探索 SGLT-2i 对非糖尿病肾脏病患者的肾脏疾病进展、心血管事件发生的影响。后续将以匹配的方法,分析药物对不同类型患者带来的酮体及其他代谢水平改变及不良安全事件发生的影响,探索新型的治疗方案及其更优适用条件。本研究将提供真实世界的临床证据,有助于临床医生作出治疗决策,造福慢性肾脏病患者,针对药物可能产生的副作用进行预防,延缓或改变疾病的最终结局来获得更佳预后。 |
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Objectives of Study: |
The aim of the study is to explore the effects of SGLT-2i on the progression of renal disease and cardiovascular events in non-diabetic kidney disease patients using real-world data. The effects of the drug on ketone bodies and other metabolic changes and adverse safety events in different types of patients will be analyzed in a matched approach to explore novel therapeutic regimens and their optimal applicability. This study will provide real-world clinical evidence that will help clinicians to make therapeutic decisions for the benefit of patients with CKD, to prevent possible side effects of medications, and to delay or alter the final outcome of the disease to achieve a better prognosis. |
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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: |
签署知情同意书时年龄必须>18 岁,临床诊断为慢性肾脏病 |
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Inclusion criteria |
Must be >18 years of age at the time of signing the informed consent form and have a clinical diagnosis of chronic kidney disease |
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排除标准: |
所有类型糖尿病 |
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Exclusion criteria: |
All types of diabetes |
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研究实施时间: Study execute time: |
从 From 2024-02-01 00:00:00至 To 2026-02-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-02-01 00:00:00 至 To 2024-05-01 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: |
无 |
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Blinding: |
None |
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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 |
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): |
不适用 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
none |
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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: |
记录表及电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF and Electronic Data Capture |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |