注册号: Registration number: |
ChiCTR2300067999 |
最近更新日期: Date of Last Refreshed on: |
2023-02-02 |
注册时间: Date of Registration: |
2023-02-02 |
注册号状态: |
补注册 |
Registration Status: |
Retrospective registration |
注册题目: |
免疫耐受期慢乙肝患者抗病毒治疗预后评估方案 |
Public title: |
Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage |
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: |
免疫耐受期慢乙肝患者抗病毒治疗预后评估方案 |
Scientific title: |
Prognosis evaluation of antiviral therapy for patients with chronic hepatitis B in immune tolerance stage |
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: |
申请注册联系人: |
张欢 |
研究负责人: |
雷学忠 |
Applicant: |
Huan Zhang |
Study leader: |
XueZhong Lei |
申请注册联系人电话: Applicant telephone: |
13755208515 |
研究负责人电话: Study leader's telephone: |
18980601317 |
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: |
1215398916@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
18980601317@163.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): |
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申请注册联系人通讯地址: |
四川省成都市武侯区国学巷37号 |
研究负责人通讯地址: |
四川省成都市武侯区国学巷37号 |
Applicant address: |
#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China |
Study leader's address: |
#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China |
申请注册联系人邮政编码: Applicant postcode: |
610041 |
研究负责人邮政编码: Study leader's postcode: |
610041 |
申请人所在单位: |
四川大学华西医院 |
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Applicant's institution: |
West China Hospital of Sichuan University |
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: |
2022年审(1126)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: |
四川大学华西医院生物医学伦理审查委员会 |
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Name of the ethic committee: |
The Biomedical Ethics Review Committee of West China Hospital, Sichuan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-07-15 | ||
伦理委员会联系人: |
彭淑贤 |
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Contact Name of the ethic committee: |
ShuXian Peng |
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伦理委员会联系地址: |
四川省成都市武侯区国学巷37号 |
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Contact Address of the ethic committee: |
#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
四川大学华西医院 |
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Primary sponsor: |
West China Hospital, Sichuan University |
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研究实施负责(组长)单位地址: |
四川省成都市武侯区国学巷37号 |
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Primary sponsor's address: |
#37 Guoxue Alley, Wuhou District, Chengdu, Sichuan Province, China |
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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: |
无 |
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Source(s) of funding: |
None |
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研究疾病: |
乙肝 |
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Target disease: |
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 | ||||||||||||||||||||||
Study phase: |
N/A |
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研究目的: |
本研究旨在研究免疫耐受期慢乙肝患者的抗病毒治疗效果,评估GP73在治疗预后中的指导意义。 |
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Objectives of Study: |
The purpose of this study was to investigate the efficacy of antiviral therapy in patients with chronic hepatitis B in immune-tolerant stage, and to evaluate the guiding significance of GP73 in treatment prognosis. |
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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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研究设计: |
队列研究 |
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Study design: |
Cohort study |
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纳入标准: |
1、HBV DNA≥ 1.00E+07 IU/ML; 2、血清HBsAg阳性至少6个月以上,且HBeAg阳性; 3、血清ALT正常或<2x ULN; 4、近3个月内Fibroscan<9.0 Kpa和肝脏彩超提示无肝硬化,或近1年内肝脏组织病理学检查无明显炎症坏死或纤维化; 5、初治或经治患者均可。 |
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Inclusion criteria |
1. HBV DNA≥ 1.00E+07 IU/ML; 2. Serum HBsAg positive for at least 6 months and HBeAg positive; 3. Serum ALT was normal or < 2x ULN; 4. No liver cirrhosis was indicated by Fibroscan < 9.0kpa and liver color ultrasound within the last 3 months, or no obvious inflammatory necrosis or fibrosis was observed by liver histopathological examination within the last 1 year; 5. All patients can be treated initially or after treatment. |
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排除标准: |
1、合并肝硬化、肿瘤、结缔组织病等; 2、排除酒精肝、药物性肝炎、自身免疫性肝炎、甲丙戊肝炎等; 3、存在心、肺、肝、肾等其他系统严重功能障碍; 4、患有严重的精神疾病,怀孕、哺乳期受试者; 5、其他研究者认为不适合参加研究的情况。 |
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Exclusion criteria: |
1. Cirrhosis, tumor, connective tissue disease, etc.; 2. Exclude alcoholic liver, drug hepatitis, autoimmune hepatitis, hepatitis A vale, etc.; 3. Serious dysfunction of heart, lung, liver, kidney and other systems; 4. Subjects with serious mental illness, pregnancy or lactation; 5. Conditions that other researchers consider unsuitable for participating in the study. |
研究实施时间: Study execute time: |
从From2022-08-01至To 2024-12-31 |
征募观察对象时间: Recruiting time: |
从From2022-08-01至To 2024-12-31 |
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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