合并高CMV血症的住院艾滋病患者的管理新策略研究

注册号:

Registration number:

ChiCTR2600126010 

最近更新日期:

Date of Last Refreshed on:

2026-06-02 14:24:38 

注册时间:

Date of Registration:

2026-06-02 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

合并高CMV血症的住院艾滋病患者的管理新策略研究

Public title:

New Strategies for the Management of Hospitalized AIDS Patients with Concurrent High CMV Viremia

注册题目简写:

English Acronym:

研究课题的正式科学名称:

合并高CMV血症的住院艾滋病患者的管理新策略研究

Scientific title:

New Strategies for the Management of Hospitalized AIDS Patients with Concurrent High CMV Viremia

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:

魏洪霞 

研究负责人:

魏洪霞 

Applicant:

Hongxia Wei 

Study leader:

Hongxia Wei 

申请注册联系人电话:

Applicant telephone:

+86 25 8509 1717

研究负责人电话:

Study leader's
telephone:

+86 25 8509 1717

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:

wghongxia@sina.com

研究负责人电子邮件:

Study leader's E-mail:

wghongxia@sina.com

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:

江苏省南京市鼓楼区钟阜路1-1号

研究负责人通讯地址:

江苏省南京市鼓楼区钟阜路1-1号

Applicant address:

No. 1-1 Zhongfu Road, Gulou District, Nanjing City, Jiangsu Province

Study leader's address:

No. 1-1 Zhongfu Road, Gulou District, Nanjing City, Jiangsu Province

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:

南京市第二医院

Applicant's institution:

The Second Hospital of Nanjing

研究负责人所在单位:

南京市第二医院

Affiliation of the Leader:

The Second Hospital of Nanjing

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:

2026-LS-ky049

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:

南京市第二医院科技伦理(审查)委员会

Name of the ethic committee:

Nanjing Second Hospital Medical Ethics Committee

伦理委员会批准日期:

Date of approved by ethic committee:

2026-04-03 00:00:00

伦理委员会联系人:

王苏娟

Contact Name of the ethic committee:

Wang Sujuan

伦理委员会联系地址:

江苏省南京市鼓楼区钟阜路1-1号

Contact Address of the ethic committee:

No. 1-1 Zhongfu Road, Gulou District, Nanjing City, Jiangsu Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 25 85091772

伦理委员会联系人邮箱:

Contact email of the ethic committee:

1058934767@qq.com

研究实施负责(组长)单位:

南京市第二医院

Primary sponsor:

The Second Hospital of Nanjing

研究实施负责(组长)单位地址:

江苏省南京市鼓楼区钟阜路1-1号

Primary sponsor's address:

No. 1-1 Zhongfu Road, Gulou District, Nanjing City, Jiangsu Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏省

市(区县):

Country:

China

Province:

Jiangsu

City:

单位(医院):

南京市第二医院

具体地址:

江苏省南京市鼓楼区钟阜路1-1号

Institution
hospital:

The Second Hospital of Nanjing

Address:

No. 1-1 Zhongfu Road, Gulou District, Nanjing City, Jiangsu Province

经费或物资来源:

艾滋病和病毒性肝炎等重大传染病防治

Source(s) of funding:

Prevention and Control of Emerging and Major Infectious Diseases-National Science and Technology Maj

研究疾病:

艾滋病  

Target disease:

AIDS

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

评估在CMV DNA升高但无靶器官表现的住院艾滋病患者中实施早期抗CMV治疗,是否可以改善6个月生存结局,降低CMV相关终末器官损害(EOD)发生率  

Objectives of Study:

Evaluate whether early anti-CMV therapy in hospitalized AIDS patients with elevated CMV DNA but no target organ manifestations can improve 6-month survival outcomes and reduce the incidence of CMV-related end-organ damage (EOD).

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.明确存在CMV EOD,包括CMV视网膜炎、CMV脑炎、CMV肺炎、CMV食管炎、CMV肠炎等;
2.合并恶性肿瘤;
3.对更昔洛韦或膦甲酸钠存在明确禁忌或严重不耐受;
4.妊娠或哺乳期女性;
5.研究者认为存在其他不适合参加试验的情况;

Exclusion criteria:

1.Confirmed presence of CMV end-organ damage (EOD), including CMV retinitis, CMV encephalitis, CMV pneumonia, CMV esophagitis, CMV enteritis, etc;
2.Concurrent malignancy;
3.Clear contraindication or severe intolerance to ganciclovir or foscarnet sodium;
4.Pregnant or breastfeeding women;
5.Other conditions deemed by the investigator to make the patient unsuitable for participation in the trial;

研究实施时间:

Study execute time:

From 2026-01-01 00:00:00 To 2028-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2026-06-08 00:00:00 To 2028-12-31 00:00:00

干预措施:

Interventions:

组别:

对照组

样本量:

220

Group:

Control group

Sample size:

干预措施:

诊断 CMV 相关 EOD 者按现有指南用药,无诊断依据者则不治疗

干预措施代码:

Intervention:

Patients diagnosed with CMV-related EOD should be treated according to existing guidelines, while those without diagnostic evidence should not be treated.

Intervention code:

组别:

试验组

样本量:

220

Group:

Experimental group

Sample size:

干预措施:

抗 CMV 治疗固定疗程 3 周,首选更昔洛韦,不耐受者改膦甲酸钠,若后续明确 EOD → 按 EOD 方案管理

干预措施代码:

Intervention:

Anti-CMV treatment has a fixed course of 3 weeks, with ganciclovir as the first choice. If not tolerated, switch to foscarnet. If subsequent EOD is confirmed → manage according to the EOD protocol.

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏省 

市(区县):

 

Country:

China

Province:

Jiangsu

City:

单位(医院):

南京市第二医院 

单位级别:

三级甲等 

Institution
hospital:

The Second Hospital of Nanjing

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

北京市 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

中国医学科学院北京协和医院 

单位级别:

三级甲等 

Institution
hospital:

Peking Union Medical College Hospita

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

广东省 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

广州医科大学附属市八医院 

单位级别:

三级医院 

Institution
hospital:

Guangzhou Eighth People's Hospital, Guangzhou Medical University

Level of the institution:

Tertiary

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

国家:

中国

省(直辖市):

广西壮族自治区 

市(区县):

 

Country:

China

Province:

Guangxi Zhuang Autonomous Region

City:

单位(医院):

广西壮族自治区胸科医院 

单位级别:

三级医院 

Institution
hospital:

Chest Hospital of Guangxi Zhuang Autonomous Region

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

四川省 

市(区县):

 

Country:

China

Province:

Sichuan

City:

单位(医院):

成都市公共卫生临床医疗中心 

单位级别:

三级医院 

Institution
hospital:

Chengdu Public Health Clinical Center

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

福建省 

市(区县):

 

Country:

China

Province:

Fujian

City:

单位(医院):

福建医科大学孟超肝胆医院 

单位级别:

三级甲等 

Institution
hospital:

Mengchao Hepatobiliary Hospital OF Fujian Medical University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

浙江省 

市(区县):

 

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江大学医学院附属第一医院 

单位级别:

三级甲等 

Institution
hospital:

The First Affiliated Hospital, Zhejiang University School of Medicine

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

重庆市 

市(区县):

 

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆市公共卫生医疗救治中心 

单位级别:

三级医院 

Institution
hospital:

Chongqing Public Health Medical Center

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

云南省 

市(区县):

 

Country:

China

Province:

Yunnan

City:

单位(医院):

昆明市第三人民医院 

单位级别:

三级医院 

Institution
hospital:

Kunming Third People's Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

贵州省 

市(区县):

 

Country:

China

Province:

Guizhou

City:

单位(医院):

贵阳市公共卫生救治中心 

单位级别:

三级医院 

Institution
hospital:

Guiyang Public Health Clinical Center

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

北京市 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

首都医科大学附属北京地坛医院 

单位级别:

三级甲等 

Institution
hospital:

Beijing Ditan Hospital, Capital Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

6个月全因病死率

指标类型:

主要指标

Outcome:

6-month all-cause mortality rate

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

免疫重建情况:CD4+T细胞计数上升幅度、HIV RNA变化

指标类型:

次要指标

Outcome:

Immune reconstitution status: magnitude of increase in CD4+ T cell count, and changes in HIV RNA.

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

不同生物样本类型(全血、血清、血浆、尿液)的CMV DNA

指标类型:

次要指标

Outcome:

The value of CMV DNA in different samples (whole blood, serum, plasma, urine) for diagnosing CMV infection, predicting clinical outcomes, and monitoring treatment.

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

早期抗CMV方案(3周)应用于高CMV病毒血症患者的病毒学抑制率及EOD发生风险

指标类型:

次要指标

Outcome:

Early anti-CMV regimen (3 weeks) for viral suppression rate and risk of EOD in patients with high CMV viremia.

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

早期抗CMV治疗策略的安全性及相关不良事件发生情况

指标类型:

次要指标

Outcome:

Safety and occurrence of related adverse events of the early anti-CMV treatment strategy.

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

尿液

组织:

Sample Name:

Urine

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

血清

组织:

Sample Name:

Serum

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

血浆

组织:

Sample Name:

Plasma

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

血液

组织:

Sample Name:

Blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 65 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):

计算机生成随机序列

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

Computer-generated random sequence

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:

开放标签

Blinding:

Open-label study

是否共享原始数据:

IPD sharing

否No

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):

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

None

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:

EDC

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

EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2026-06-02 14:24:20