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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: |
ChiCTR2500108806 |
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最近更新日期: Date of Last Refreshed on: |
2025-09-05 16:21:31 |
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注册时间: Date of Registration: |
2025-09-05 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: |
面向医生的糖尿病及并发症智能决策系统的有效性临床研究 |
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Public title: |
Clinical Research on the Effectiveness of Doctor oriented Intelligent Decision System for diabetes and Complications |
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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: |
面向医生的糖尿病及并发症智能决策系统的有效性临床研究 |
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Scientific title: |
Clinical Research on the Effectiveness of Doctor oriented Intelligent Decision System for diabetes and Complications |
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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: |
王楚媛 |
研究负责人: |
单忠艳 |
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Applicant: |
Chuyuan Wang |
Study leader: |
Zhongyan Shan |
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申请注册联系人电话: Applicant telephone: |
+86 138 8981 0509 |
研究负责人电话: Study leader's telephone: |
+86 138 0490 5018 |
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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: |
chuyuan0215@163.com |
研究负责人电子邮件: Study leader's E-mail: |
shanzhongyan@medmail.com.cn |
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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: |
辽宁省沈阳市和平区南京北街155号 |
研究负责人通讯地址: |
辽宁省沈阳市和平区南京北街155号 |
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Applicant address: |
No. 155, Nanjing North Street, Heping District, Shenyang City, Liaoning Province |
Study leader's address: |
No. 155, Nanjing North Street, Heping District, Shenyang City, Liaoning Province |
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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: |
中国医科大学附属第一医院 |
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Applicant's institution: |
The First Hospital of China Medical University |
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研究负责人所在单位: |
中国医科大学附属第一医院 |
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Affiliation of the Leader: |
The First Hospital of China Medical 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: |
[2025]2025-683-2 |
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: |
中国医科大学附属第一医院医学科学研究伦理委员会 |
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Name of the ethic committee: |
Ethics Committee for Medical Scientific Research, First Hospital of China Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-08-25 00:00:00 |
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伦理委员会联系人: |
王印博 |
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Contact Name of the ethic committee: |
Yinbo Wang |
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伦理委员会联系地址: |
辽宁省沈阳市和平区南京北街155号 |
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Contact Address of the ethic committee: |
No. 155, Nanjing North Street, Heping District, Shenyang City, Liaoning Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 24 8328 2837 |
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: |
中国医科大学附属第一医院 |
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Primary sponsor: |
The First Hospital of China Medical University |
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研究实施负责(组长)单位地址: |
辽宁省沈阳市和平区南京北街155号 |
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Primary sponsor's address: |
No. 155, Nanjing North Street, Heping District, Shenyang City, Liaoning Province |
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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: |
癌症、心脑血管、呼吸和代谢性疾病防治研究国家科技重大专项 |
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Source(s) of funding: |
National Major Scientific and Technological Special Project for Cancer, Cardiovascular and Cerebrovascular, Respiratory, and Metabolic Disease Prevention and Treatment Research |
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Target disease: |
Diabetes |
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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: |
开展全国多中心随机对照临床研究,与标准诊疗相比,评估智能化管理新技术对糖尿病及并发症管理的有效性。 |
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Objectives of Study: |
Conduct a nationwide multi-center randomized controlled clinical study to evaluate the effectiveness of new intelligent management technologies in managing diabetes and its complications, compared to standard diagnosis and treatment. |
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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、确诊2型糖尿病; 2、年龄在40~70岁; 3、能够接受人工智能辅助诊疗的糖尿病管理模式; 4、能够提供完整的医疗记录,包括病史、用药情况等; 5、充分了解研究目的、性质、方法,自愿进入本研究,接受为期24个月的随访, 并签署知情同意书。 |
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Inclusion criteria |
1. Type 2 diabetes; 2. Age between 40 and 70 years old; 3. Able to accept the artificial intelligence assisted diagnosis and treatment of diabetes management mode; 4. Capable of providing complete medical records, including medical history, medication use, etc; 5. Fully understand the research purpose, nature, and methods, voluntarily enter this study, undergo a 24 month follow-up, and sign an informed consent form. |
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排除标准: |
1、存在严重精神疾病或语言障碍; 2、患有恶性肿瘤; 3、妊娠或哺乳期女性; 4、疑似活动性感染者(如活动性肺结核、肺炎等); 5、严重肝肾功能不全(谷丙转氨酶和(或)谷草转氨酶>正常上限3倍,估算 的肾小球滤过率<15 mL/min/1.73 m2); 6、既往有明确的主要不良心血管事件和(或)行血运重建和(或)静脉溶栓 治疗和(或)血管内取栓治疗; 7、已明确诊断的非糖尿病视网膜病变及非糖尿病肾病; 8、未控制的甲状腺功能亢进或甲状腺功能减退、垂体肾上腺功能异常等其他 内分泌疾病; 9、酗酒或药物成瘾; 10、因各种原因(如个人信仰、经济因素等)无法接受综合干预新技术者。 |
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Exclusion criteria: |
1. Having severe mental illness or language impairment; 2. Suffering from malignant tumor; 3. Pregnant or lactating women; 4. Individuals with suspected active infections (such as active tuberculosis, pneumonia, etc.); 5. Severe hepatic and renal insufficiency (alanine aminotransferase and/or aspartate aminotransferase > 3 times the upper limit of normal, estimated) glomerular filtration rate (GFR) < 15 mL/min/1.73 m2); 6. Previous history of definite major adverse cardiovascular events and/or undergoing revascularization and/or intravenous thrombolysis Treatment and/or intravascular thrombus removal therapy; 7. Definitely diagnosed non-diabetic retinopathy and non-diabetic nephropathy; 8. Uncontrolled hyperthyroidism or hypothyroidism, pituitary-adrenal dysfunction, and other conditions Endocrine diseases; 9. Alcoholism or drug addiction; 10. Those who, for various reasons (such as personal beliefs, economic factors, etc.), cannot accept new comprehensive intervention technologies. |
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研究实施时间: Study execute time: |
从 From 2024-08-01 00:00:00至 To 2028-07-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2025-09-05 00:00:00 至 To 2028-07-31 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: |
正在进行 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): |
面向医生的糖尿病及并发症智能决策系统的有效性临床研究,采用整群随机的方法,系统将临床水平相近的医院随机1:1分为标准诊疗组或智能辅助决策组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Clinical research on the effectiveness of physician oriented intelligent decision-making system for diabetes and complications. The system randomly divides hospitals with similar clinical levels into standard diagnosis and treatment group or intelligent assistant decision-making group 1:1 by adopting the cluster random method |
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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: |
开放标签 |
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Blinding: |
Open label |
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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): |
网络平台https://deepdms.com/login,试验结束六个月后再提交 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The online platform https://deepdms.com/login and submit six months after the trial ends |
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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: |
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: |
Electronic Data Capture, EDC |
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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 |