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注册号: Registration number: |
ChiCTR2600119032 |
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最近更新日期: Date of Last Refreshed on: |
2026-02-14 09:49:57 |
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注册时间: Date of Registration: |
2026-02-14 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
一项在中国1型糖尿病先证者的一级亲属中评估1型糖尿病疾病进展风险的多中心、前瞻性纵向研究 |
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Public title: |
A Multi-center, Prospective Longitudinal Study to Assess the Risk of Disease Progression of Type 1 Diabetes in First-degree Relatives of Type 1 Diabetes Probands in China |
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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: |
一项在中国1型糖尿病先证者的一级亲属中评估1型糖尿病疾病进展风险的多中心、前瞻性纵向研究 |
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Scientific title: |
A Multi-center, Prospective Longitudinal Study to Assess the Risk of Disease Progression of Type 1 Diabetes in First-degree Relatives of Type 1 Diabetes Probands in China |
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研究课题代号(代码): Study subject ID: |
OBS18677 |
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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: |
杨雪 |
研究负责人: |
郭立新 |
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Applicant: |
Xue Yang |
Study leader: |
Lixin Guo |
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申请注册联系人电话: Applicant telephone: |
+86 10 6563 4716 |
研究负责人电话:
Study leader's |
+86 139 0131 7569 |
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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: |
Contact-US.CN@sanofi.com |
研究负责人电子邮件: Study leader's E-mail: |
glx1218@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: |
中国上海市静安区延安中路1228号嘉里中心3座19层 |
研究负责人通讯地址: |
北京市东城区东单大华路1 号 |
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Applicant address: |
19F, Tower III, Kerry Center, 1228 Middle Yan’an Road, Jing An District, Shanghai, China |
Study leader's address: |
No. 1 Dongdan Dahua Road, Dongcheng District, Beijing |
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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: |
赛诺菲(中国)投资有限公司上海分公司 |
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Applicant's institution: |
Sanofi (China) Investment Co., Ltd. Shanghai Branch |
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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-KY187-02 |
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: |
Beijing Hospital Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-09-11 00:00:00 | ||
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伦理委员会联系人: |
秦梓淋 |
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Contact Name of the ethic committee: |
Zilin Qin |
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伦理委员会联系地址: |
北京市东城区东单大华路1 号 |
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Contact Address of the ethic committee: |
No. 1 Dongdan Dahua Road, Dongcheng District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 5811 5035 |
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: |
北京市东城区东单大华路1 号 |
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Primary sponsor's address: |
No. 1 Dongdan Dahua Road, Dongcheng District, Beijing |
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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: |
赛诺菲(中国)投资有限公司上海分公司 |
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Source(s) of funding: |
Sanofi (China) Investment Co., Ltd. Shanghai Branch |
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研究疾病: |
1型糖尿病 |
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Target disease: |
Type 1 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: |
观察性研究 |
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Study type: |
Observational 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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
主要目的: 评估T1D先证者的自身抗体阳性FDR在5年内发生3期T1D的风险。 次要目的: 1. 在T1D先证者的FDR中评估自身抗体阳性率。 2. 在自身抗体阳性FDR中评估疾病进展至T1D不同分期的风险。 3. 评估早期T1D受试者的β细胞功能和血糖结局。 4. 通过评估诊断后前12个月内的临床特征、自身抗体、β细胞功能和血糖结局,探索T1D的异质性。 |
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Objectives of Study: |
Primary objectives: To assess the risk of Stage 3 T1D onset during the 5 years in autoantibody positive FDRs of T1D probands. Secondary objectives: 1. To assess the autoantibody positivity in FDRs of T1D probands. 2. To assess the risk of disease progression to different stages of T1D in autoantibody positive FDRs. 3. To assess the beta cell function and glycaemic outcomes in early stage T1D participants. 4. To explore T1D heterogeneity, as assessed by clinical characteristics, autoantibodies, beta cell function and glycaemic outcomes, during the first 12 months from diagnosis. |
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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: |
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Inclusion criteria |
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排除标准: |
1.已根据ADA诊断标准,临床上诊断为糖尿病,包括但不限于T1D、2型糖尿病(T2D)、单基因糖尿病、妊娠糖尿病(GDM)和其他。 2.先证者患有T2D、单基因糖尿病或继发于另一种疾病的糖尿病。 3.既往或当前使用控制高血糖症的药物(例如胰岛素、口服降糖药)。 4.目前正在使用全身免疫抑制或免疫调节治疗(局部和吸入性药物除外)。 5.患有任何已知的严重活动性疾病和/或可能导致预期寿命有限或需要在研究期间使用免疫抑制或免疫调节治疗的其他疾病。 6.根据研究者的判断,具有可能会导致受试者因数据解读问题或安全性问题而不符合入选资格的任何病史或临床相关异常。 7.预期不依从方案。 8.正在参加干预性研究或其他药物的试验性研究,可能会影响这项研究的主要目的。 9.妊娠或哺乳期女性。 |
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Exclusion criteria: |
1. Have been clinically diagnosed with diabetes according to the ADA diagnostic criteria, including but not limited to T1D, type 2 diabetes (T2D), monogenic diabetes, gestational diabetes (GDM), and others. 2. The affected probands has T2D, monogenic diabetes, or diabetes secondary to another medical condition. 3. Have previous or current use of medications for the control of hyperglycaemia (e.g., insulin, oral hypoglycaemic agents). 4. Currently be using systemic immunosuppressive or immunomodulatory therapies (topical and inhaled agents are acceptable). 5. Have any known severe active diseases, and/or other diseases which are likely to limit life expectancy or lead to the use of immunosuppressive or immunomodulatory therapies during the study. 6. Any medical history or clinically relevant abnormality that is deemed by the investigator to make the participant ineligible for inclusion because problems in interpreting data or safety concern. 7. Expected non-compliance with the protocol. 8. Participating in interventional or other drug research studies which could affected the primary objectives of the study. 9. Pregnant or lactating women. |
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研究实施时间: Study execute time: |
从 From 2025-12-09 00:00:00至 To 2034-12-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-12-09 00:00:00 至 To 2027-12-30 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): |
None |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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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: |
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Blinding: |
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
试验结束后,可通过提交请求至https://vivli.org,获取个体受试者数据和支持性临床文档。在提供信息时,赛诺菲将始终保护临床试验受试者的隐私。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Individual participant data and supporting clinical documents are available for request at vivli.org. While making information available we continue to protect the privacy of study participants. |
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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: |
CRF和EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF & EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |