ChiCTR2400089257 版本V1.0 版本创建时间2024/09/04 14:54:10 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:

ChiCTR2400089257 

最近更新日期:

Date of Last Refreshed on:

2024-09-04 14:54:04 

注册时间:

Date of Registration:

2024-09-04 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

富马酸丙酚替诺福韦在乙肝低病毒血症患者的疗效及安全性研究

Public title:

Efficacy and safety of tenofovir alafenamide in CHB patients with low-level viraemia

注册题目简写:

English Acronym:

研究课题的正式科学名称:

富马酸丙酚替诺福韦在乙肝低病毒血症患者的疗效及安全性研究

Scientific title:

Efficacy and safety of tenofovir alafenamide in CHB patients with low-level viraemia

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:

贺梦雯 

研究负责人:

纪冬 

Applicant:

He Mengwen 

Study leader:

Ji Dong 

申请注册联系人电话:

Applicant telephone:

+86 135 1227 6377

研究负责人电话:

Study leader's telephone:

+86 138 0126 1069

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:

hemengwen99@163.com

研究负责人电子邮件:

Study leader's E-mail:

jidg302@126.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:

中国北京市西四环中路100号(邮政编码100039)

研究负责人通讯地址:

中国北京市西四环中路100号(邮政编码100039)

Applicant address:

100 Western 4th Ring Middle Road, Beijing 100039, China

Study leader's address:

100 Western 4th Ring Middle Road, Beijing 100039, China

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:

解放军总医院第五医学中心肝病医学部

Applicant's institution:

Senior Department of Hepatology, the Fifth Medical Center of PLA General Hospital

研究负责人所在单位:

解放军总医院第五医学中心肝病医学部

Affiliation of the Leader:

Senior Department of Hepatology, the Fifth Medical Center of PLA General Hospital

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2020056D

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:

中国人民解放军总医院第五医学中心医学伦理委员会

Name of the ethic committee:

The Fifth Medical Center Ethics Committee of Chinese PLA General Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2020-07-14 00:00:00

伦理委员会联系人:

于峰

Contact Name of the ethic committee:

Feng Yu

伦理委员会联系地址:

中国北京市丰台区西四环中路100号

Contact Address of the ethic committee:

100 Western 4th Ring Middle Road, Beijing 100039, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 10 106 693 3460

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

解放军总医院第五医学中心

Primary sponsor:

The Fifth Medical Center of Chinese PLA General Hospital

研究实施负责(组长)单位地址:

中国北京市丰台区西四环中路100号

Primary sponsor's address:

100 Western 4th Ring Middle Road, Beijing 100039, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

北京

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

解放军总医院第五医学中心

具体地址:

中国北京市丰台区西四环中路100号

Institution
hospital:

The Fifth Medical Center of Chinese PLA General Hospital

Address:

100 Western 4th Ring Middle Road, Beijing 100039, China

经费或物资来源:

国家重点研发计划项目(2023YFC2306800)

Source(s) of funding:

The National Key Research and Development Program of China (Grand No. 2023YFC2306800)

Target disease:

Chronic hepatitis B

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

我们旨在评估低病毒血症的慢性乙型肝炎患者从恩替卡韦(ETV)转用富马酸丙酚替诺福韦片(TAF)的有效性和安全性。  

Objectives of Study:

We aimed to evaluate the effectiveness and safety of switching from entecavir (ETV) to tenofovir alafenamide fumarate (TAF) in chronic hepatitis B patients with low-level viraemia.

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) 年龄超过 18 岁; (2) 血清中 HBsAg 和 HBV DNA 均呈阳性; (3) 接受 ETV 治疗超过 48 周且出现低病毒血症(HBV DNA 20-2000 IU/mL)的患者。

Inclusion criteria

(1) aged over 18 years; (2) serum positive for both HBsAg and HBV DNA; (3) ETV-treated patients who received ETV for >48 weeks and experienced LLV (HBV DNA 20-2000 IU/mL).

排除标准:

(1) 接受过其他核苷酸类似物(NUC)或聚乙二醇化干扰素-α(IFN-α)治疗; (2) 临床依从性差; (3) 同时感染丙型肝炎病毒或人类免疫缺陷病毒; (4) 合并其他肝病,包括自身免疫性肝病、药物性肝损伤等; (5) 肝硬化失代偿期(如并发明显腹水、静脉曲张出血或脑病); (6) 罹患任何癌症; (7) 怀孕或哺乳期妇女。

Exclusion criteria:

(1) treated with other nucleos(t)ide analogues (NUCs) or pegylated interferon-α (IFN-α); (2) poor clinical compliance; (3) coinfected with either hepatitis C virus or human immunodeficiency virus; (4) combined with other liver disease including autoimmune liver disease, drug-induced liver injury, etc.; (5) had decompensated cirrhosis (eg, complicated with obvious ascites, variceal haemorrhage or encephalopathy); (6) any cancers; (7) women with pregnancy or breastfeeding.

研究实施时间:

Study execute time:

From 2020-08-01 00:00:00 To 2023-08-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-09-02 00:00:00 To 2022-09-23 00:00:00  

干预措施:

Interventions:

组别:

试验组

样本量:

200

Group:

experimental group

Sample size:

干预措施:

改用 TAF(25 mg/天)疗法

干预措施代码:

Intervention:

switching to TAF (25 mg/d) therapy

Intervention code:

组别:

对照组

样本量:

200

Group:

control group

Sample size:

干预措施:

继续接受 ETV(0.5 mg/天)治疗

干预措施代码:

Intervention:

continuing ETV (0.5 mg/d) therapy

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China 

Province:

Beijing 

City:

 

单位(医院):

解放军总医院第五医学中心 

单位级别:

三甲 

Institution
hospital:

Senior Department of Hepatology, the Fifth Medical Center of PLA General Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

完全病毒学应答率

指标类型:

主要指标

Outcome:

Complete virological response (CVR) 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:

血清 HBV DNA 水平下降的程度

指标类型:

次要指标

Outcome:

Degree of serum HBV DNA levels decreased

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

ALT复常率

指标类型:

次要指标

Outcome:

ALT normalization

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

血清 qHBsAg水平下降的程度

指标类型:

次要指标

Outcome:

Degree of qHBsAg decline

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

HBeAg 消失和血清转换

指标类型:

次要指标

Outcome:

HBeAg loss and seroconversion

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肝脏硬度值(LSM)、APRI与FIB-4指数的变化

指标类型:

次要指标

Outcome:

changes in liver fibrosis as measured by LSM, APRI and FIB-4

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:

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:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 80 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):

参与者未进行随机分组,而是在听取了关于两种疗法的成本、有效性、安全性和长期疗效的解释后,所有入组患者都可以根据个人意愿选择治疗方案。

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

Participants were not randomly assigned to the ETV or TAF groups. After receiving explanations of the costs, effectiveness, safety, and long-term outcomes of both therapies, all enrolled patients were allowed to choose their preferred treatment option based on their individual preferences and understanding.

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:

是否共享原始数据:

IPD sharing

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):

ResMan (www.medresman.org.cn)

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

ResMan (www.medresman.org.cn)

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:

电子采集和管理系统

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:

无/No

注册人:

Name of Registration:

 2024-09-04 14:54:04