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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: |
ChiCTR2600122927 |
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最近更新日期: Date of Last Refreshed on: |
2026-04-20 14:07:21 |
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注册时间: Date of Registration: |
2026-04-20 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: |
2型糖尿病个体化诊疗新方案效果评价及策略优化--全国多中心RCT研究:辅助决策支持系统联合长效DPP-4酶抑制剂考格列汀在MARD型中的效果评价 |
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Public title: |
Evaluation of the Effectiveness and Strategy Optimization of a New Individualized Diagnosis and Treatment Plan for Type 2 Diabetes Mellitus: A National Multicenter RCT Study - Evaluation of the Effectiveness of an Auxiliary Decision Support System Combined with the Long-Acting DPP-4 Enzyme Inhibitor Cofrogliptin in MARD Type |
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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: |
2型糖尿病个体化诊疗新方案效果评价及策略优化--全国多中心RCT研究:辅助决策支持系统联合长效DPP-4酶抑制剂考格列汀在MARD型中的效果评价 |
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Scientific title: |
Evaluation of the Effectiveness and Strategy Optimization of a New Individualized Diagnosis and Treatment Plan for Type 2 Diabetes Mellitus: A National Multicenter RCT Study - Evaluation of the Effectiveness of an Auxiliary Decision Support System Combined with the Long-Acting DPP-4 Enzyme Inhibitor Cofrogliptin in MARD Type |
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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: |
张洁 |
研究负责人: |
潘琦 |
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Applicant: |
Jie Zhang |
Study leader: |
Qi Pan |
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申请注册联系人电话: Applicant telephone: |
+86 186 1140 7002 |
研究负责人电话:
Study leader's |
+86 189 0133 0621 |
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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: |
18611407002@163.com |
研究负责人电子邮件: Study leader's E-mail: |
panqi621@126.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: |
中国北京东城区东单大华路1号 |
研究负责人通讯地址: |
中国北京东城区东单大华路1号 |
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Applicant address: |
1 Dahua Road, Dongdan, Dongcheng District, Beijing, China |
Study leader's address: |
1 Dahua Road, Dongdan, Dongcheng District, Beijing, 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: |
北京医院 |
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Applicant's institution: |
Beijing Hospital |
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研究负责人所在单位: |
北京医院 |
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Affiliation of the Leader: |
Beijing Hospital |
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是否获伦理委员会批准: |
是 |
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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: |
2025BJYYEC-KY125-02 |
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: |
北京医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Beijing Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-07-08 00:00:00 | ||
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伦理委员会联系人: |
侯文静 |
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Contact Name of the ethic committee: |
Wenjing Hou |
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伦理委员会联系地址: |
中国北京东城区东单大华路1号 |
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Contact Address of the ethic committee: |
1 Dahua Road, Dongdan, Dongcheng District, Beijing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 8513 8522 |
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: |
北京医院 |
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Primary sponsor: |
Beijing Hospital |
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研究实施负责(组长)单位地址: |
中国北京东城区东单大华路1号 |
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Primary sponsor's address: |
1 Dahua Road, Dongdan, Dongcheng District, Beijing, 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: |
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 Science and Technology Major Project on the Prevention and Treatment of Cancer, Cardiovascular and Cerebrovascular Diseases, Respiratory and Metabolic Diseases |
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研究疾病: |
糖尿病 |
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Target disease: |
Diabetes |
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研究疾病代码: |
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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: |
针对现有降糖药物在不同糖尿病分型患者中疗效不明确、控制率低的问题,本研究通过全国多中心RCT研究,探讨辅助决策支持系统联合长效DPP-4抑制剂考格列汀在MARD型糖尿病患者中的疗效。 |
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Objectives of Study: |
In view of the unclear efficacy and low control rate of existing hypoglycemic drugs in patients with different types of diabetes, this study conducted a multi-center RCT across the country to explore the efficacy of the decision support system combined with the long-acting DPP-4 inhibitor Koglitin in patients with MARD-type diabetes. |
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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.年龄 60 岁以上; 2.近 1 年内新确诊为 2 型糖尿病; 3.入组前 3 个月内仅接受 DPP-4 抑制剂日制剂和(或)二甲双胍治疗; 4.入组前3 个月内 FPG<15mmol/L 且 HbA1c≤10.5%。 5.能够理解本试验的程序和方法,愿意遵守临床研究方案完成本试验,并自愿签署知情同意书 |
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Inclusion criteria |
1. Age over 60 years old; 2. Newly diagnosed with type 2 diabetes within the past year; 3.Only received DPP-4 inhibitor daily preparations and/or metformin treatment within the 3 months prior to enrollment; 4.FPG < 15 mmol/L and HbA1c <= 10.5% within the 3 months prior to enrollment. 5. Able to understand the procedures and methods of this trial, willing to comply with the clinical research protocol to complete this trial, and voluntarily sign the informed consent form. |
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排除标准: |
1.入组前6 个月内发生过糖尿病急性事件; 2.患有严重疾病(如癌症、HIV、严重外周血 管疾病、各类免疫系统疾病、严重精神疾患或语言障碍); 3.入组前 6 个月内使用其他可能影响血糖代谢的药物(如全身性糖皮质激素、生长激素等); 4.入组前 3 个月内发生急性冠脉综合征、卒中或短暂性脑缺血发作,入组前有药物不可 控制的高血压(如收缩压≥160mmHg,舒张压≥90mmHg); 5.正在参与其他临床实验; 6.其他研究者判断存在不适合参加本研究的其他情况等。 |
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Exclusion criteria: |
1. Participants who had experienced acute diabetic events within 6 months before enrollment; 2.Those with severe diseases (such as cancer, HIV, severe peripheral vascular disease, various immune system diseases, severe mental disorders or language barriers); 3. Those who had used other drugs that might affect glucose metabolism within 6 months before enrollment (such as systemic glucocorticoids, growth hormones, etc.); 4. Those who had experienced acute coronary syndrome, stroke or transient ischemic attack within 3 months before enrollment, or had uncontrolled hypertension (such as systolic blood pressure ≥ 160mmHg, diastolic blood pressure ≥ 90mmHg) before enrollment; 5.Those who were participating in other clinical trials; 6. Other situations deemed unsuitable for participation in this study by the researchers. |
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研究实施时间: Study execute time: |
从 From 2026-02-07 00:00:00至 To 2029-01-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-04-25 00:00:00 至 To 2027-01-01 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): |
根据随机数字表和入组时间顺序随机 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Randomized according to the random number table and the order of enrollment time. |
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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 |
否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): |
N/A |
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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,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: |
Case record form, electronic collection and management system |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |