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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: |
ChiCTR2500108331 |
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最近更新日期: Date of Last Refreshed on: |
2025-08-28 14:52:46 |
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注册时间: Date of Registration: |
2025-08-28 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: |
使用聚乙二醇干扰素a-2b治疗核苷(酸)类似物(NAs)经治低HBsAg水平的HBeAg阳性慢性乙型肝炎患者的多中心、单臂、观察性临床研究123@(审核员标记请勿删除:1、多中心参研单位列表与研究方案合并成一个文档上传!!!2、将完整首例和末例参试者知情同意书脱密处理(将姓名、电话盖住,只保留签字日期以确认征募时间)与空白版知情同意书(版本号、日期、格式必须一致)合并成一个文档上传!3、中英文对照填写注册表!!!核对注册表,确保填写内容与研究方案一致!!4、补注册研究,必须完善填写共享原始数据的方式与时间,EDC或者具有公式功能的网址都可以,但必须填写;)使用聚乙二醇干扰素a-2b治疗核苷(酸)类似物(NAs)经治HBsAg<3000 IU/mL 的HBeAg阳性慢性乙型肝炎患者的多中心、前瞻性临床研究 |
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Public title: |
A multicenter, single-arm, observational clinical study on the treatment of HBeAg-positive chronic hepatitis B patients with low HBsAg levels who have been treated with nucleoside (acid) analogues (NAs) using peginterferon alfa-2b. |
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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: |
使用聚乙二醇干扰素a-2b治疗核苷(酸)类似物(NAs)经治低HBsAg水平的HBeAg阳性慢性乙型肝炎患者的多中心、单臂、观察性临床研究 |
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Scientific title: |
A multicenter, single-arm, observational clinical study on the use of polyethylene glycol interferon alpha-2b in the treatment of HBeAg-positive chronic hepatitis B patients with low HBsAg levels who have been treated with nucleoside (acid) analogs (NAs) |
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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: |
胡克珍 |
研究负责人: |
辛永宁 |
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Applicant: |
Hu Kezhen |
Study leader: |
Xin Yongning |
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申请注册联系人电话: Applicant telephone: |
+86 152 1645 2396 |
研究负责人电话:
Study leader's |
+86 186 6167 8200 |
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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: |
hukezhen2000@163.com |
研究负责人电子邮件: Study leader's E-mail: |
xinyongning@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: |
山东省青岛市市北区胶州路1号 |
研究负责人通讯地址: |
山东省青岛市市北区胶州路1号 |
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Applicant address: |
No. 1 Jiaozhou Road, Shibei District, Qingdao City, Shandong Province |
Study leader's address: |
No. 1 Jiaozhou Road, Shibei District, Qingdao City, Shandong Province |
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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: |
青岛大学 青岛市市立医院 |
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Applicant's institution: |
Qingdao University Qingdao Municipal Hospital |
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研究负责人所在单位: |
青岛市市立医院 |
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Affiliation of the Leader: |
Qingdao Municipal 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: |
2023临审字第Y004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: |
青岛市市立医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Qingdao Municipal Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-02-22 00:00:00 | ||
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伦理委员会联系人: |
王国安 |
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Contact Name of the ethic committee: |
Wang Guoan |
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伦理委员会联系地址: |
山东省青岛市市北区胶州路1号 |
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Contact Address of the ethic committee: |
No. 1 Jiaozhou Road, Shibei District, Qingdao City, Shandong Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 176 6975 7920 |
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: |
青岛市市立医院 |
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Primary sponsor: |
Qingdao Municipal Hospital |
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研究实施负责(组长)单位地址: |
山东省青岛市市北区胶州路1号 |
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Primary sponsor's address: |
No. 1 Jiaozhou Road, Shibei District, Qingdao City, Shandong Province |
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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: |
国家自然科学基金(项目编号:32171277、82202416)、中国肝炎预防控制基金会穆欣慢性乙型肝炎研究基金(项目编号:MX202409)、北京 iGandan 基金会临床研究项目(iGandanF-1082024-LG002)、青岛医学与健康研究指导项目(项目编号:2023-WJZD173)、青岛重点医学与健康学科项目。 |
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Source(s) of funding: |
National Natural Science Foundation of China (32171277, 82202416), the China Hepatitis Prevention and Control Foundation Mu Xin Chronic Hepatitis B Research Fund (MX202409), the Beijing iGandan Foundation Clinical Research Project (iGandanF-1082024-LG002), the Qingdao Medical and Health Research Guidance Project (2023-WJZD173), Qingdao Key Medical and Health Discipline Project. |
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研究疾病: |
慢性乙肝病毒肝炎 |
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Target disease: |
Chronic hepatitis B |
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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: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
本究旨在评估聚乙二醇化干扰素-α2b(PEG-IFNα-2b)在核苷(酸)类似物经治性、HBeAg 阳性且基线时 HBsAg 低于 3000 IU/ml的慢性乙型肝炎患者中的疗效和安全性,从而为这一亚组患者的干扰素治疗提供依据。 |
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Objectives of Study: |
This study aimed to evaluate the efficacy and safety of pegylated interferon-α2b (PEG-IFNα-2b) in NA-experienced, HBeAg-positive CHB patients with baseline HBsAg <3000 IU/mL, providing evidence to guide interferon-based therapy in this subgroup. |
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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.自愿入组,能理解和签署知情同意书; 2.年龄18-65岁(包括18和65),性别不限; 3.HBsAg阳性病史至少6个月或其他证据提示为慢性乙型肝炎; 4.基线HBsAg<1000IU/mL;HBV DNA<500IU/ml; 5.基线HBeAg阳性; 6.NAs至少连续使用12个月; 7.患者符合干扰素治疗指征,预期接受聚乙二醇干扰素α-2b治疗。 |
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Inclusion criteria |
1. Voluntarily enrolled, able to understand and sign the informed consent form; 2. Age 18-65 years old (including 18 and 65), gender is not limited; 3. History of HBsAg positivity for at least 6 months or other evidence suggestive of chronic hepatitis B; 4. Baseline HBsAg< 1000IU/mL; HBV DNA<500IU/ml; 5. Baseline HBeAg positive; 6. NAs for at least 12 consecutive months; 7. Patient meets indications for interferon therapy and is expected to receive treatment with pegylated interferon α-2b. |
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排除标准: |
1.合并甲肝、丙肝、丁肝、戊肝和/或HIV现症感染; 2.其他原因引起的慢性肝病,如酒精性肝炎、药物性肝炎、自身免疫性肝病、中重度脂肪性肝炎及肝细胞癌; 3.研究期间拟接受替比夫定治疗者; 4.研究期间计划使用具有抗HBV疗效的其它药物(包括中草药); 5.研究者认为不适宜入组的其他情况。 |
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Exclusion criteria: |
1. Combined with hepatitis A, hepatitis C, hepatitis D, hepatitis E and/or HIV infection; 2. Chronic liver diseases caused by other causes, such as alcoholic hepatitis, drug-induced hepatitis, autoimmune liver disease, moderate to severe steatohepatitis and hepatocellular carcinoma; 3. Those who plan to receive telbivudine treatment during the study period; 4. Planned use of other drugs with anti-HBV efficacy (including Chinese herbal medicine) during the study; 5. Other situations that the investigator considers unsuitable for enrollment. |
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研究实施时间: Study execute time: |
从 From 2022-02-22 00:00:00至 To 2025-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-03-02 00:00:00 至 To 2024-11-30 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: |
结束 /Completed |
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: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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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): |
ResMan,论文发表后一年内, http://www.medresman.org.cn/login.aspx。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
ResMan, within one year of publication, http://www.medresman.org.cn/login.aspx. |
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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: |
有/Yes |