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注册号: Registration number: |
ChiCTR2400082602 |
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最近更新日期: Date of Last Refreshed on: |
2024-04-01 17:22:12 |
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注册时间: Date of Registration: |
2024-04-01 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
以ΔHBsAg水平为指导的长效干扰素治疗HBeAg阴性的慢性HBV感染者的真实世界研究 |
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Public title: |
A real-world study of long-acting interferon guided by ΔHBsAg levels in the treatment of HBeAg-negative patients with chronic HBV infection |
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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: |
以ΔHBsAg水平为指导的长效干扰素治疗HBeAg阴性的慢性HBV感染者的真实世界研究 |
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Scientific title: |
A real-world study of long-acting interferon guided by ΔHBsAg levels in the treatment of HBeAg-negative patients with chronic HBV infection |
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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: |
邵彤彤 |
研究负责人: |
鲁晓擘 |
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Applicant: |
Shao Tongtong |
Study leader: |
Lu Xiaobo |
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申请注册联系人电话: Applicant telephone: |
+86 157 3950 0732 |
研究负责人电话:
Study leader's |
+86 159 9917 6213 |
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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: |
392213109@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
xjykdluxiaobo@126.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: |
新疆维吾尔自治区新市区新医路393号 |
研究负责人通讯地址: |
新疆维吾尔自治区新市区新医路393号 |
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Applicant address: |
No. 393, Xinyi Road, Xinshi District, Xinjiang Uygur Autonomous R |
Study leader's address: |
No. 393, Xinyi Road, Xinshi District, Xinjiang Uygur Autonomous R |
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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: |
新疆医科大学第一附属医院 |
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Applicant's institution: |
The First Affiliated Hospital of Xinjiang Medical University |
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研究负责人所在单位: |
新疆医科大学第一附属医院 |
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Affiliation of the Leader: |
The First Affiliated Hospital of Xinjiang Medical University |
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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: |
K202402-04 |
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: |
新疆医科大学第一附属医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Xinjiang Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-02-08 00:00:00 | ||
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伦理委员会联系人: |
汤宝鹏 |
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Contact Name of the ethic committee: |
Tang Baopeng |
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伦理委员会联系地址: |
新疆维吾尔自治区新市区新医路393号 |
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Contact Address of the ethic committee: |
No. 393, Xinyi Road, Xinshi District, Xinjiang Uygur Autonomous Region |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 187 9053 1290 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
1002717250@qq.com |
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研究实施负责(组长)单位: |
新疆医科大学第一附属医院 |
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Primary sponsor: |
The First Affiliated Hospital of Xinjiang Medical University |
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研究实施负责(组长)单位地址: |
新疆维吾尔自治区新市区新医路393号 |
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Primary sponsor's address: |
No. 393, Xinyi Road, Xinshi District, Xinjiang Uygur Autonomous Region |
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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: |
新疆医科大学第一附属医院 |
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Source(s) of funding: |
The First Affiliated Hospital of Xinjiang Medical University |
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研究疾病: |
慢性乙型病毒型肝炎 |
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Target disease: |
Chronic viral 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: |
上市后药物 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Study phase: |
4 |
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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: |
旨在建立以△HBsAg水平为指导的长效干扰素治疗HBeAg阴性的慢性HBV感染者的真实世界研究 |
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Objectives of Study: |
To establish a real-world study of long-acting interferon guided by △HBsAg level in the treatment of HBeAg-negative chronic HBV infected persons |
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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: |
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Inclusion criteria |
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排除标准: |
(1)短期内有妊娠计划、精神病史(具有精神分裂症或严重抑郁症等病史)、未能控制的癫痫、失代偿期肝硬化、未控制的自身免疫病,及严重感染、视网膜疾病、心力衰竭、慢性阻塞性肺病等基础疾病。 (2)合并甲肝、丙肝、丁肝、戊肝和/或 HIV 现症感染,或合并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; (3)恶性肿瘤者,或有任何器官移植史以及现存的功能性移植物(角膜或毛发移植除外); (4)对派格宾过敏者,或符合试验用药品说明书中任何一条禁忌症者; (5)研究者认为不适合参加本研究的受试者。 |
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Exclusion criteria: |
(1) Short-term pregnancy plans, a history of mental illness (such as schizophrenia or severe depression), uncontrolled epilepsy, decompensated cirrhosis, uncontrolled autoimmune diseases, and underlying diseases such as severe infections, retinal diseases, heart failure, and chronic obstructive pulmonary disease. (2) combined with hepatitis A, C, D, E and/or HIV infection, or with other causes of chronic liver disease, such as alcoholic hepatitis, drug-induced hepatitis, autoimmune liver disease; (3) malignant tumors, or any history of organ transplantation and existing functional grafts (other than corneal or hair transplants); (4) persons who are allergic to pygabine, or who meet any contraindication in the instruction manual of the experimental drug; (5) Subjects deemed unsuitable for this study by the researcher. |
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研究实施时间: Study execute time: |
从 From 2024-04-01 00:00:00至 To 2027-04-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-04-01 00:00:00 至 To 2027-04-01 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: |
尚未开始 Not yet 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): |
本研究为前瞻性队列观察性真实世界研究,接诊患者的临床医生根据指南、自身经验和患者意愿进行临床决策,根据患者的基线情况和选择的方案对患者进行分类入组,进入不同队列接受观察随访。统计分析使用SPSS21、MedCalc、SAS软件进行。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This study is a prospective cohort observational real-world study. Clinicians who receive patients make clinical decisions based on guidelines, their own experience, and patients' wishes. Patients are classified into different cohorts for observation and follow-up according to their baseline conditions and selected protocols. Statistical analysis was performed using SPSS21, MedCalc and SAS software. |
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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 |
否No |
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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): |
不共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not shared |
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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: |
应用Epidata制作标准的临床数据收集电子表格,双人独立录入,对不一致数据进行第三人核对,保证原始数据真实可靠。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
data collection spreadsheet, two people entered it independently, and the inconsistent data were checked by the third party to ensure the authenticity and reliability of the original data |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |