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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: |
ChiCTR2600120590 |
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最近更新日期: Date of Last Refreshed on: |
2026-03-17 10:11:15 |
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注册时间: Date of Registration: |
2026-03-17 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: |
基于肠道菌群调控探索大豆蛋白植物性膳食改善CKD慢性低度炎症的效应研究 |
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Public title: |
Exploring the Effect of Soy Protein Plant-Based Diets on Improving Chronic Low-Grade Inflammation in CKD Based on Gut Microbiota Regulation |
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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: |
基于肠道菌群调控探索大豆蛋白植物性膳食改善CKD慢性低度炎症的效应研究 |
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Scientific title: |
Exploring the Effect of Soy Protein Plant-Based Diets on Improving Chronic Low-Grade Inflammation in CKD Based on Gut Microbiota Regulation |
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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: |
田荣荣 |
研究负责人: |
田荣荣 |
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Applicant: |
Tian Rongrong |
Study leader: |
Tian Rongrong |
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申请注册联系人电话: Applicant telephone: |
+86 571 85827571 |
研究负责人电话: Study leader's telephone: |
+86 571 85827571 |
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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: |
missingy@163.com |
研究负责人电子邮件: Study leader's E-mail: |
missingy@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: |
中国浙江省杭州市西湖区体育场路453号 |
研究负责人通讯地址: |
中国浙江省杭州市西湖区体育场路453号 |
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Applicant address: |
No. 453, Stadium Road, Xihu District, Hangzhou, Zhejiang, China |
Study leader's address: |
No. 453, Stadium Road, Xihu District, Hangzhou, Zhejiang, 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: |
杭州市中医院 |
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Applicant's institution: |
Hangzhou Hospital of Traditional Chinese Medicine |
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研究负责人所在单位: |
杭州市中医院 |
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Affiliation of the Leader: |
Hangzhou Hospital of Traditional Chinese Medicine |
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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: |
2025KLL193 |
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: |
杭州市中医院科研伦理委员会 |
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Name of the ethic committee: |
Scientific Research Ethics Committee of Hangzhou TCM Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-09-24 00:00:00 |
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伦理委员会联系人: |
张来 |
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Contact Name of the ethic committee: |
Zhang Lai |
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伦理委员会联系地址: |
中国浙江省杭州市西湖区体育场路453号 |
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Contact Address of the ethic committee: |
No. 453, Stadium Road, Xihu District, Hangzhou, Zhejiang, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 571 85827896 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
623063093@qq.com |
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研究实施负责(组长)单位: |
杭州市中医院 |
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Primary sponsor: |
Hangzhou Hospital of Traditional Chinese Medicine |
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研究实施负责(组长)单位地址: |
中国浙江省杭州市西湖区体育场路453号 |
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Primary sponsor's address: |
No. 453, Stadium Road, Xihu District, Hangzhou, Zhejiang, 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: |
浙江省医药卫生计划 |
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Source(s) of funding: |
Zhejiang Medical and Health Program |
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Target disease: |
Chronic kidney disease |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional 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: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
(1)结合宏基因组学、炎症标志物及屏障功能检测等多组学手段,旨在揭示大豆蛋白主导的植物性膳食模式对于“肠道菌群-屏障-炎症”的改善作用;(2)为CKD治疗提供一种安全、有效、可持续且符合地域饮食文化的膳食模式,助力实现CKD患者的“靶向抗炎”与长期健康获益。 |
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Objectives of Study: |
(1) By integrating multi-omics approaches, including metagenomics, inflammatory marker analysis, and barrier function assays, this study aims to elucidate the ameliorative effects of a soy protein-dominated plant-based diet on the "gut microbiota-barrier-inflammation" axis. (2) The goal is to provide a safe, effective, sustainable, and culturally appropriate dietary strategy for CKD treatment, facilitating targeted anti-inflammatory therapy and promoting long-term health benefits for patients. |
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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: |
1.CKD3-4期(15mL/min/1.73m^2≤GFR≤60 mL/min/1.73m^2); 2.年龄18-75岁,性别不限; 3.理解和阅读能力正常的患者; 4.自愿参加研究并签署知情同意书的患者; |
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Inclusion criteria |
1.Patients with CKD stages 3-4 (15 mL/min/1.73 m^2 <= eGFR <= 60 mL/min/1.73 m^2); 2.Aged 18-75 years, regardless of gender; 3.Patients with normal comprehension and reading ability; 4.Patients who voluntarily participate in the study and provide signed informed consent; |
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排除标准: |
1.合并其他严重疾病者,如恶性肿瘤、严重肝功能障碍(ALT或AST>2.5ULN)、消化道出血、造血系统严重原发性疾病者;严重高血压(收缩压≥200mmHg,舒张压≥120mmHg)并且血压难以控制者;严重营养不良(SGA评分为C级)者;严重低蛋白血症,白蛋白<30g/L者; |
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Exclusion criteria: |
1.Patients with other serious comorbidities, such as malignant tumors, severe liver dysfunction (ALT or AST > 2.5 × ULN), gastrointestinal bleeding, severe primary hematopoietic system diseases; severe hypertension (systolic BP >= 200 mmHg or diastolic BP >= 120 mmHg) that is difficult to control; severe malnutrition (SGA score of C); or severe hypoproteinemia (albumin < 30 g/L); 2.History of acute cardiovascular or cerebrovascular events within the last 6 months, such as myocardial infarction, heart failure, unstable angina, transient ischemic attack, or stroke; 3.History of systemic infectious diseases within the last month; 4.Patients expected to require dialysis within 3 months; 5.Women who are lactating or pregnant; 6.Concurrent participation in other clinical trials; 7.Any other medical or psychological condition that, in the investigator’s judgment, makes the patient unsuitable for participation in this study; |
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研究实施时间: Study execute time: |
从 From 2026-01-01 00:00:00至 To 2028-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2026-04-01 00:00:00 至 To 2026-12-31 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): |
通过计算机生成随机序列实现1:1分配。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Randomization was performed by means of a computer-generated sequence, with a 1:1 allocation ratio |
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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: |
不公开/Private |
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盲法: |
开放标签,对评估者隐藏分组 |
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Blinding: |
Open-label study with blinded-evaluators |
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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): |
无 |
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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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form, CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |