ChiCTR2500103257 版本V1.0 版本创建时间2025/05/27 11:45:48 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:

ChiCTR2500103257 

最近更新日期:

Date of Last Refreshed on:

2025-05-27 11:45:01 

注册时间:

Date of Registration:

2025-05-27 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

非奈利酮治疗与2型糖尿病肾病患者血清信号素3C的相关性

Public title:

Correlation between the treatment of finerenone and serum semaphorin 3C in patients with type 2 diabetes nephropathy

注册题目简写:

English Acronym:

研究课题的正式科学名称:

非奈利酮治疗2型糖尿病肾病的临床研究

Scientific title:

The study of finerenone in the treatment of type 2 diabetic nephropathy

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:

王雅静 

研究负责人:

张真稳 

Applicant:

Yajing Wang 

Study leader:

Zhenwen Zhang 

申请注册联系人电话:

Applicant telephone:

+86 158 3018 7605

研究负责人电话:

Study leader's telephone:

+86 189 2190 1233

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:

908645519@qq.com

研究负责人电子邮件:

Study leader's E-mail:

yzdxzzw@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:

江苏省扬州市广陵区南通西路98号

研究负责人通讯地址:

江苏省扬州市广陵区南通西路98号

Applicant address:

No.98 Nantong West Road, Yangzhou City, Jiangsu Province, Yangzhou

Study leader's address:

No.98 Nantong West Road, Yangzhou City, Jiangsu Province, Yangzhou

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:

江苏省苏北人民医院

Applicant's institution:

Northern Jiangsu People's Hospital

研究负责人所在单位:

江苏省苏北人民医院

Affiliation of the Leader:

Northern Jiangsu People's Hospital

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2024ky019

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:

苏北人民医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Northern Jiangsu People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2024-01-31 00:00:00

伦理委员会联系人:

仲伟

Contact Name of the ethic committee:

Wei Zhong

伦理委员会联系地址:

江苏省扬州市广陵区南通西路98号

Contact Address of the ethic committee:

No.98 Nantong West Road, Yangzhou City, Jiangsu Province, Yangzhou

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 514 8737 3415

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

江苏省苏北人民医院

Primary sponsor:

Northern Jiangsu People's Hospital

研究实施负责(组长)单位地址:

江苏省扬州市广陵区南通西路98号

Primary sponsor's address:

No.98 Nantong West Road, Yangzhou City, Jiangsu Province, Yangzhou

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏

市(区县):

扬州

Country:

China

Province:

Jiangsu

City:

Yangzhou

单位(医院):

江苏省苏北人民医院

具体地址:

江苏省扬州市广陵区南通西路98号

Institution
hospital:

Northern Jiangsu People's Hospital

Address:

No.98 Nantong West Road, Yangzhou City, Jiangsu Province, Yangzhou

经费或物资来源:

自筹

Source(s) of funding:

self-finance

Target disease:

Type 2 diabetes nephropathy

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:

横断面 

Study design:

Cross-sectional 

研究目的:

探究非奈利酮治疗2型糖尿病肾病的疗效及对血清、尿液SEMA3C水平和纤维化指标的影响,为2型糖尿病肾病的治疗提供新的思路。  

Objectives of Study:

To investigate the efficacy of finerenone in the treatment of type 2 diabetic nephropathy and its effect on serum and urinary SEMA3C levels and fibrosis indexes, and to provide new ideas for the treatment of type 2 diabetic nephropathy.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

所有入选者需符合1999年WHO糖尿病诊断标准:具有典型糖尿病症状(口干、多饮、多尿,不明原因的体重下降)者符合其中一条: (1)随机血糖≥11.1 mmol/L;(2)空腹血浆血糖≥7.0 mmol/L;(3)口服葡萄糖耐量试验二小时后血浆血糖≥11.1 mmol/L。无典型症状者需不同日再测一次。 糖尿病肾病采用2021年《中国糖尿病肾脏疾病防治临床指南》中的诊断标准:至少具备下列中的一项:(1)eGFR低于60ml·min-1·(1.73m2)-1持续超过3个月;(2)尿白蛋白/肌酐比值高于30mg/g持续超过3个月;(3)肾活检符合DKD的病理改变。 存在下列状况时考虑肾脏病的病因为非糖尿病所致:(1)1型糖尿病病程短(<10年)或未合并糖尿病视网膜病变;(2)eGFR迅速下降;(3)尿蛋白迅速增加或出现肾病综合征;(4)顽固性高血压;(5)出现活动性尿沉渣红细胞、白细胞或细胞管型等;(6)合并其他系统性疾病的症状或体征;(7)给予血管紧张素转化酶抑制剂或血管紧张素受体拮抗剂治疗后2~3个月内eGFR下降大于30%;(8)肾脏超声发现异常。

Inclusion criteria

All participants were required to meet the 1999 WHO diagnostic criteria for diabetes mellitus: those with typical diabetic symptoms (dry mouth, excessive drinking and urination, unexplained weight loss) met one of the criteria: (1) random blood glucose >=11.1 mmol/L; (2) fasting plasma glucose >=7.0 mmol/L; (3) plasma glucose >=11.1 mmol/L after two hours of oral glucose tolerance test; those with no typical symptoms need to be measured again on a different day. Diabetic nephropathy is diagnosed according to the 2021 Chinese Clinical Guidelines for the Prevention and Treatment of Diabetic Kidney Disease: at least one of the following: (1) eGFR less than 60 ml-min-1-(1.73 m2)-1 for more than 3 months; (2) urinary albumin/creatinine ratio more than 30 mg/g for more than 3 months; and (3) renal biopsy consistent with the pathologic changes of DKD. The etiology of renal disease was considered to be non-diabetic in the presence of the following conditions: (1) type 1 diabetes mellitus with a short duration of illness (<10 years) or without comorbid diabetic retinopathy; (2) a rapid decline in eGFR; (3) a rapid increase in urinary proteins or the development of a nephrotic syndrome; (4) refractory hypertension; (5) the presence of active urinary sediment erythrocytes, leukocytes, or cellular tubular patterns; and (6) the comorbidity with other systemic signs or symptoms of disease; (7) a decrease in eGFR greater than 30% within 2 to 3 months after administration of angiotensin-converting enzyme inhibitors or angiotensin receptor antagonists; and (8) abnormal renal ultrasound findings.

排除标准:

其他原发性肾脏疾病;除2型糖尿病以外的其他类型糖尿病;糖尿病酮症酸中毒、高血糖高渗综合征、糖尿病乳酸酸中毒等糖尿病急性并发症;严重感染等应激状态;自身免疫系统、血液系统疾病或恶性肿瘤;心功能不全、肝功能异常及严重的心脑血管疾病;严重的精神疾病或智力障碍;应用其他醛固酮受体拮抗剂患者。

Exclusion criteria:

Other primary renal diseases; other types of diabetes except type 2 diabetes mellitus; acute complications of diabetes mellitus such as diabetic ketoacidosis, hyperglycemic hyperosmolar syndrome, diabetic lactic acidosis; severe infections and other stress conditions; autoimmune system, hematologic disorders, or malignant tumors; cardiac insufficiency, hepatic abnormalities, and severe cardiovascular and cerebral vascular disorders; severe psychiatric disorders or mental retardation; and the use of other aldosterone receptor antagonist patients.

研究实施时间:

Study execute time:

From 2024-01-31 00:00:00 To 2025-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-06-01 00:00:00 To 2025-12-31 00:00:00  

干预措施:

Interventions:

组别:

2型糖尿病肾病组

样本量:

60

Group:

Type 2 diabetic nephropathy group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

非奈利酮组

样本量:

60

Group:

Finerenone group

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):

江苏 

市(区县):

 

Country:

China 

Province:

Jiangsu 

City:

 

单位(医院):

江苏省苏北人民医院 

单位级别:

三甲 

Institution
hospital:

Northern Jiangsu People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

SEMA3C

指标类型:

主要指标

Outcome:

SEMA3C

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

C肽

指标类型:

次要指标

Outcome:

c peptide

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

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:

标本中文名:

尿液

组织:

Sample Name:

urine

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 years
最大 Max age 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:

公开/Public

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

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):

不共享

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:

病例记录表

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

Case Record Form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2025-05-27 11:45:01