ChiCTR2600124427 版本V1.0 版本创建时间2026/05/12 12:03:16 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2600124427 

最近更新日期:

Date of Last Refreshed on:

2026-05-12 12:03:04 

注册时间:

Date of Registration:

2026-05-12 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

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

Public title:

Prospective Observational Cohort Study on the Metabolic Effects of Different ART Regimens in Chinese HIV-Infected Individuals

注册题目简写:

English Acronym:

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

Scientific title:

Prospective Observational Cohort Study on the Metabolic Effects of Different ART Regimens in Chinese HIV-Infected Individuals

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:

顾玲 

研究负责人:

沈银忠 

Applicant:

Gu Ling 

Study leader:

Shen Yinzhong 

申请注册联系人电话:

Applicant telephone:

+86 21 37990333

研究负责人电话:

Study leader's
telephone:

+86 21 37990333

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:

guling@shaphc.org

研究负责人电子邮件:

Study leader's E-mail:

shenyinzhong@shphc.org.cn

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):

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

Applicant address:

No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai

Study leader's address:

No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai

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:

申请人所在单位:

上海市公共卫生临床中心

Applicant's institution:

Shanghai Public Health Clinical Center

研究负责人所在单位:

上海市公共卫生临床中心

Affiliation of the Leader:

Shanghai Public Health Clinical Center

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:

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

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

Name of the ethic committee:

Shanghai Public Health Clinical Center Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2025-07-23 00:00:00

伦理委员会联系人:

刘晓茜

Contact Name of the ethic committee:

Liu Xiaoqian

伦理委员会联系地址:

上海市金山区山阳镇漕廊公路2901号

Contact Address of the ethic committee:

No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai

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

研究实施负责(组长)单位:

上海市公共卫生临床中心

Primary sponsor:

Shanghai Public Health Clinical Center

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

Primary sponsor's address:

No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海市

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市公共卫生临床中心

具体地址:

上海市金山区山阳镇漕廊公路2901号

Institution
hospital:

Shanghai Public Health Clinical Center

Address:

No. 2901, Caolang Highway, Shanyang Town, Jinshan District, Shanghai

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

Source(s) of funding:

Shanghai Clinical Cohort Project of Shanghai Shenkang Hospital Development Center

研究疾病:

艾滋病  

Target disease:

AIDS

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

连续入组 

Study design:

Sequential 

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)。  

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.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1.年龄≥18岁;
2.确诊HIV感染并启动ART≥6个月;
3.基线未诊断为MetS;
4.能够理解并遵守研究方案要求,且自愿签署书面的知情同意书者;

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;

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);

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.);

研究实施时间:

Study execute time:

From 2025-07-01 00:00:00 To 2027-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-08-04 00:00:00 To 2027-12-31 00:00:00

干预措施:

Interventions:

组别:

D组

样本量:

250

Group:

D group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

C组

样本量:

250

Group:

C group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

B组

样本量:

250

Group:

B group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

A组

样本量:

250

Group:

A group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

上海市 

市(区县):

 

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市公共卫生临床中心 

单位级别:

三级甲等 

Institution
hospital:

Shanghai Public Health Clinical Center

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

接受不同 ART 治疗方案各亚组的 HIV 感染者代谢综合征(MetS) 的发生率,以及代谢相关指标的变化(腹型肥胖、血压、空腹血糖、TG、HDL-C)

指标类型:

主要指标

Outcome:

Incidence of metabolic syndrome (MetS) in HIV-infected individuals in different subgroups receiving various ART regimens, and changes in metabolism-related indicators (abdominal obesity, blood pressure, fasting blood glucose, TG, HDL-C)

Type:

Primary indicator

测量时间点:

入组后 12、24 个月

测量方法:

Measure time point of outcome:

12 and 24 months after enrollment

Measure method:

指标中文名:

代谢相关指标(腹型肥胖、血压、空腹血糖、TG、HDL- C)的变化值

指标类型:

次要指标

Outcome:

Changes in metabolism-related indicators (abdominal obesity, blood pressure, fasting blood glucose, TG, HDL-C)

Type:

Secondary indicator

测量时间点:

6 个月、12、24 个月

测量方法:

Measure time point of outcome:

6 months, 12 months, 24 months

Measure method:

指标中文名:

HIV RNA<50 copies/ml 的患者比例,及 CD4+ T 细胞、 CD8 + T 细胞、CD4 + /CD8+比值较基线的变化值

指标类型:

次要指标

Outcome:

The proportion of patients with HIV RNA <50 copies/ml, and the changes from baseline in CD4 T cells, CD8 T cells, and the CD4/CD8 ratio

Type:

Secondary indicator

测量时间点:

12个月、24个月

测量方法:

Measure time point of outcome:

12, 24 months

Measure method:

指标中文名:

抗病毒治疗失败、转换治疗方案比例以及患者依从性

指标类型:

次要指标

Outcome:

Proportion of antiviral treatment failure, therapy regimen change, and patient adherence

Type:

Secondary indicator

测量时间点:

12个月、24个月

测量方法:

Measure time point of outcome:

12 months, 24 months

Measure method:

指标中文名:

与基线相比肝肾功能的变化

指标类型:

次要指标

Outcome:

Changes in liver and kidney function compared to baseline

Type:

Secondary indicator

测量时间点:

12个月、24个月

测量方法:

Measure time point of outcome:

12 months, 24 months

Measure method:

指标中文名:

不良事件(AE)发生率

指标类型:

次要指标

Outcome:

Incidence of adverse events (AE)

Type:

Secondary indicator

测量时间点:

12个月、24个月

测量方法:

Measure time point of outcome:

12 months, 24 months

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 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):

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

None

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:

Blinding:

None

是否共享原始数据:

IPD sharing

是Yes

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。

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.

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

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

CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2026-05-12 12:03:04