恒格列净对2型糖尿病并心脏自主神经病变的随机对照研究

注册号:

Registration number:

ChiCTR2500101113 

最近更新日期:

Date of Last Refreshed on:

2025-04-21 09:56:05 

注册时间:

Date of Registration:

2025-04-21 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

恒格列净对2型糖尿病并心脏自主神经病变的随机对照研究

Public title:

A randomized controlled study of Henagliflozin in type 2 diabetes mellitus with cardiac autonomic neuropathy

注册题目简写:

English Acronym:

研究课题的正式科学名称:

新型SGLT2抑制剂对2型糖尿病并心脏自主神经病变的随机对照研究

Scientific title:

A randomized controlled study of novel SGLT2 inhibitors in type 2 diabetes mellitus with cardiac autonomic neuropathy

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:

傅晓莹 

研究负责人:

傅晓莹 

Applicant:

Fu Xiaoying 

Study leader:

Fu Xiaoying 

申请注册联系人电话:

Applicant telephone:

+86 135 6009 5467

研究负责人电话:

Study leader's
telephone:

+86 135 6009 5467

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:

fuxy126@163.com

研究负责人电子邮件:

Study leader's E-mail:

fuxy126@163.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

内分泌科

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:

广州市中山二路106号广东省人民医院主体楼19楼

研究负责人通讯地址:

广州市中山二路106号广东省人民医院主体楼19楼

Applicant address:

Guangdong Provincial People's Hospital, 106 Zhongshan Second Road, Guangzhou

Study leader's address:

Guangdong Provincial People's Hospital, 106 Zhongshan Second Road, Guangzhou

申请注册联系人邮政编码:

Applicant postcode:

510080

研究负责人邮政编码:

Study leader's postcode:

510080

申请人所在单位:

广东省人民医院(广东省医学科学院)

Applicant's institution:

Guangdong Provincial People's Hospital (Guangdong Provincial Academy of Medical Sciences)

研究负责人所在单位:

广东省人民医院(广东省医学科学院)

Affiliation of the Leader:

Guangdong Provincial People's Hospital (Guangdong Provincial Academy of Medical Sciences)

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

KY2024-836-01; KY2024-836-03

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:

广东省人民医院伦理审查委员会

Name of the ethic committee:

Ethics Review Committee of Guangdong Provincial People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2024-10-28 00:00:00

伦理委员会联系人:

白胜

Contact Name of the ethic committee:

Bai Sheng

伦理委员会联系地址:

广州市越秀区东华南路98号,海印中心23F

Contact Address of the ethic committee:

Haiyin Center, 98 East South Road, Yuexiu District, Guangzhou

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 20 8352 5173

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:

广东省人民医院

Primary sponsor:

Guangdong Provincial People's Hospital

研究实施负责(组长)单位地址:

越秀区中山二路106号

Primary sponsor's address:

No. 106, Zhongshan er Road

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

广东

市(区县):

广州市

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

广东省人民医院

具体地址:

越秀区中山二路106号

Institution
hospital:

Guangdong Provincial People's Hospital

Address:

No. 106, Zhongshan er Road

经费或物资来源:

国家卫生健康委医药卫生科技发展研究中心

Source(s) of funding:

National Health Commission Medical Science and Technology development research center

研究疾病:

糖尿病  

Target disease:

diabetes

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要目的:观察SGLT2i恒格列净对2型糖尿病心脏自主神经病变(CAN)的疗效,探 讨治疗2型糖尿病心脏自主神经功能紊乱的新方案。 次要目的:评价恒格列净治疗T2DM患者CAN的安全性;优化CAN的诊断方法。  

Objectives of Study:

Objective: To observe the effect of SGLT2i Henagliflozin on type 2 diabetic cardiac autonomic neuropathy (CAN) to discuss a new scheme for the treatment of cardiac autonomic nervous dysfunction in type 2 diabetes. Secondary objective: To evaluate the safety of Henagliflozin in the treatment of CAN in T2DM patients;Optimize the diagnosis method of CAN.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

① 肝功能受损[丙氨酸氨基转移酶(ALT)或门冬氨酸氨基转移酶(AST)>3倍正常上限]; ② 未控制的不稳定或稳定型心绞痛,ECG或血清血提示心肌缺血,6个月内发生过心肌梗死、脑卒中、严重心功能不全(NYHA心功能Ⅲ-Ⅳ级)等心血管事件; ③ 甲状腺功能异常; ④ 慢性阻塞性肺病; ⑤ 增殖性视网膜病变; ⑥ 控制不佳的高血压(收缩压>180mmHg或舒张压>100mmHg); ⑦ 非糖尿病导致的CAN,如帕金森病、多系统萎缩、肌萎缩侧索硬化、自身免疫性疾病(如干燥综合征)等可能导致CAN的疾病; ⑧ 安装心脏起搏器; ⑨ 已知的频发性(>6次/min)或持续性心律失常; ⑩ 3个月内使用过SGLT2i或GLP-1 RA类药物; ⑪ 处于发热、感染、脱水、低血糖或严重高血糖状态[空腹血糖(FPG)>13.9mmol/L或糖化血红蛋白(HbA1c)>12%]状态; ⑫ 酗酒(长期饮酒>5年,折合乙醇量男性≥40g/d,女性≥20 g/d,或2周内有大量 饮酒史,折合乙醇量>80 g/d); ⑬ 妊娠状态或未来1年内有妊娠计划; ⑭ 对SGLT2i类药物过敏。

Exclusion criteria:

1. Impaired liver function [alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 3 times normalUpper limit]; 2.Uncontrolled unstable or stable angina pectoris, ECG or serum blood indicates myocardial ischemia, and a heart attack occurs within 6 months Myocardial infarction, stroke, severe cardiac insufficiency (NYHA grade Ⅲ-Ⅳ) and other cardiovascular events; 3.Abnormal thyroid function; 4. Chronic obstructive pulmonary disease; 5. Proliferative retinopathy; 6.Poorly controlled hypertension (systolic blood pressure > 180mmHg or diastolic blood pressure > 100mmHg); 7. Non-diabetic CAN, such as Parkinson's disease, multiple system atrophy, amyotrophic lateral sclerosis, autoimmune diseases (such as Sjogren's syndrome) that may cause CAN; 8. Install a pacemaker; 9. Known frequent (> 6 beats /min) or persistent arrhythmias; 10. Have used SGLT2i or GLP-1 RA drugs within 3 months; 11. LIn the state of fever, infection, dehydration, hypoglycemia or severe hyperglycemia [fasting Lblood glucose (FPG) > 13.9mmol/L] Or hemoglobin a1c (HbA1c) > 12%]; 12. Binge drinking (long-term alcohol consumption > 5 years, equivalent to alcohol levels of >=40g/d for males and >=20 g/d for females, or large amounts within 2 weeks Alcohol consumption history, equivalent alcohol content >80 g/d); 13. If you are pregnant or have a pregnancy plan within the next 1 year; 14. Allergic to SGLT2i drugs.

研究实施时间:

Study execute time:

From 2025-03-01 00:00:00 To 2027-10-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-05-06 00:00:00 To 2026-12-31 00:00:00

干预措施:

Interventions:

组别:

试验组

样本量:

47

Group:

experimental group

Sample size:

干预措施:

恒格列净

干预措施代码:

Intervention:

Henagliflozin

Intervention code:

组别:

对照组

样本量:

47

Group:

control group

Sample size:

干预措施:

标准治疗(除外SGLT2和GLP-1受体激动剂)

干预措施代码:

Intervention:

Standard treatment (excluding SGLT2 inhibitors and GLP-1 receptor agonists)

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

广东省人民医院 

单位级别:

三甲 

Institution
hospital:

Guangdong Provincial People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

心率变异性

指标类型:

主要指标

Outcome:

HRV,Heart Rate Variability

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

心脏自主神经功能CARTs评分

指标类型:

主要指标

Outcome:

Cardiac autonomic function CARTs score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血糖相关指标

指标类型:

次要指标

Outcome:

Blood sugar-related indicators

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血脂谱[总胆固醇、甘油三脂、高密度脂蛋白、低密度脂蛋白)

指标类型:

次要指标

Outcome:

Lipid profile (total cholesterol, triglycerides, HDL, LDL)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

心脏彩超指标(左室射血分数(Left Ventricular Ejection Fraction,LVEF)、室间隔厚度和左室后壁厚度]

指标类型:

次要指标

Outcome:

Cardiac ultrasound index (Left Ventricular Ejection Fraction (LVEF), Ventricular septal thickness, and left ventricular posterior wall thickness)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

不良事件发生率

指标类型:

副作用指标

Outcome:

Incidence of adverse events

Type:

Adverse events

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:

组织:

Sample Name:

None

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

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 30 years
最大 Max age 75 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):

由第三方统计单位通过SAS统计软件编程实现,按照区组竞争的动态区组随机方法,给定种子数和区组长度;通过动态随机长度的区组对区组长度进行隐藏,并按 1:1 比例将受试者分为试验组和对照组。

Randomization Procedure (please state who generates the random number sequence and by what method):

By the third party statistical unit through SAS statistical software programming, according to the dynamic block random method of block competition, given the number of seeds and block length; The length of the block was hidden by the dynamic random length block, and the subjects were divided into experimental group and control group in a 1:1 ratio.

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:

单盲(研究对象不知道,研究者可查询分组)

Blinding:

single-blind

是否共享原始数据:

IPD sharing

否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):

Don't share

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:

电子采集和管理系统

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

Electronic Data Capture

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:

 2025-04-21 09:51:50