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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: |
ChiCTR2600124427 |
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最近更新日期: Date of Last Refreshed on: |
2026-05-12 12:03:04 |
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注册时间: Date of Registration: |
2026-05-12 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: |
不同ART方案对中国HIV感染者代谢影响的前瞻性、观察性队列研究 |
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Public title: |
Prospective Observational Cohort Study on the Metabolic Effects of Different ART Regimens in Chinese HIV-Infected Individuals |
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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: |
不同ART方案对中国HIV感染者代谢影响的前瞻性、观察性队列研究 |
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Scientific title: |
Prospective Observational Cohort Study on the Metabolic Effects of Different ART Regimens in Chinese HIV-Infected Individuals |
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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: |
顾玲 |
研究负责人: |
沈银忠 |
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Applicant: |
Gu Ling |
Study leader: |
Shen Yinzhong |
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申请注册联系人电话: Applicant telephone: |
+86 21 37990333 |
研究负责人电话:
Study leader's |
+86 21 37990333 |
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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: |
guling@shaphc.org |
研究负责人电子邮件: Study leader's E-mail: |
shenyinzhong@shphc.org.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: |
上海市金山区山阳镇漕廊公路2901号 |
研究负责人通讯地址: |
上海市金山区山阳镇漕廊公路2901号 |
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Applicant address: |
No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai |
Study leader's address: |
No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai |
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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: |
上海市公共卫生临床中心 |
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Applicant's institution: |
Shanghai Public Health Clinical Center |
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研究负责人所在单位: |
上海市公共卫生临床中心 |
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Affiliation of the Leader: |
Shanghai Public Health Clinical Center |
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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: |
公卫伦审2025-S093-01号 |
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: |
上海市公共卫生临床中心伦理委员会 |
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Name of the ethic committee: |
Shanghai Public Health Clinical Center Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-07-23 00:00:00 | ||
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伦理委员会联系人: |
刘晓茜 |
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Contact Name of the ethic committee: |
Liu Xiaoqian |
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伦理委员会联系地址: |
上海市金山区山阳镇漕廊公路2901号 |
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Contact Address of the ethic committee: |
No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 37990333 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
lunliweiyuanhui2009@126.com |
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研究实施负责(组长)单位: |
上海市公共卫生临床中心 |
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Primary sponsor: |
Shanghai Public Health Clinical Center |
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研究实施负责(组长)单位地址: |
上海市金山区山阳镇漕廊公路2901号 |
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Primary sponsor's address: |
No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai |
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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: |
上海申康医院发展中心上海临床队列项目 |
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Source(s) of funding: |
Shanghai Clinical Cohort Project of Shanghai Shenkang Hospital Development Center |
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研究疾病: |
艾滋病 |
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Target disease: |
AIDS |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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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: |
1. 建立HIV感染者的代谢指标研究队列,观察使用不同核心药物(核苷类逆转录酶抑制剂、非核苷逆转录酶抑制剂、蛋白酶抑制剂、整合酶抑制剂)组成的ART方案的HIV感染者代谢综合征(MetS)发生情况; 2. 比较使用不同ART方案的HIV感染者代谢异常的人群分布及动态变化(确诊MetS、代谢指标异常但未达MetS诊断标准、代谢指标正常亚组)。 |
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Objectives of Study: |
1. Establish a research cohort for metabolic indicators in HIV-infected individuals to observe the incidence of Metabolic Syndrome (MetS) in those receiving ART regimens composed of different core drugs (nucleoside reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, protease inhibitors, and integrase inhibitors); 2. Compare the population distribution and dynamic changes of metabolic abnormalities (subgroups of confirmed MetS, abnormal metabolic indicators not meeting the MetS diagnostic criteria, and normal metabolic indicators) among HIV-infected individuals on different ART regimens. |
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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≥18岁; |
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Inclusion criteria |
1.Age >= 18 years old; 2.Confirmed HIV infection and initiation of ART for >= 6 month; 3.Not diagnosed with MetS at baseline; 4.Individuals who can understand and comply with the requirements of the research protocol and voluntarily sign a written informed consent form; |
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排除标准: |
1.合并严重机会性感染(如活动性结核、隐球菌脑膜炎)或肿瘤; 2.患有精神分裂症、癫痫、重度抑郁/焦虑等重大神经及精神疾病; 3.有吸毒史、近期有酒精或药物依赖史者; 4.对研究药物的任何成分或辅料有过敏史或高敏体质者; 5.妊娠或哺乳期妇女;未采取研究者认为有效的避孕措施(例如避孕隔膜;避孕套;宫内节育器等;伴侣输精管结扎)的育龄女性; 6.处于感染性疾病的活动期、严重心血管疾病急性期等研究者认为不适合参加研究者; 7.基线eGFR<60 mL/min/1.73m^2或糖尿病史; 8.其他研究者认为不适合参加研究者(如说明书列明的禁忌与不适合人群等); |
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Exclusion criteria: |
1.Complicated with severe opportunistic infections (such as active tuberculosis, cryptococcal meningitis) or tumors; 2.Suffering from major neurological and psychiatric diseases such as schizophrenia, epilepsy, and severe depression/anxiety; 3.People with a history of drug abuse or a recent history of alcohol or drug dependence; 4.People with a history of allergies to any ingredient or excipient of the study drug, or those with a hypersensitive constitution. 5.Pregnant or lactating women; women of childbearing age who have not adopted contraceptive measures considered effective by the researcher (such as diaphragms, condoms, intrauterine devices, etc.; partner's vasectomy); 6.Individuals in the active phase of infectious diseases, the acute phase of severe cardiovascular diseases, or other conditions that the researcher deems unsuitable for participation in the study; 7.Baseline eGFR < 60 mL/min/1.73m^2 or a history of diabetes; 8.Individuals deemed unsuitable for participation in the study by the researcher for other reasons (such as contraindicated populations and unsuitable populations specified in the instruction manual, etc.); |
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研究实施时间: Study execute time: |
从 From 2025-07-01 00:00:00至 To 2027-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-08-04 00:00:00 至 To 2027-12-31 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): |
无 |
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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: |
无 |
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Blinding: |
None |
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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): |
研究完成后,计划在保护研究参与者隐私的情况下,将数据共享在ResMan平台。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the study is completed, the data will be shared on the ResMan platform while protecting the privacy of the research 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: |
病例记录表 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |