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注册号: Registration number: |
ChiCTR2400085066 |
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最近更新日期: Date of Last Refreshed on: |
2024-05-30 15:04:08 |
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注册时间: Date of Registration: |
2024-05-30 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: |
慢性 HBV 感染孕妇产后临床治愈研究 |
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Public title: |
The study on clinical cure of postpartum pregnant women 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: |
慢性 HBV 感染孕妇产后临床治愈研究 |
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Scientific title: |
The study on clinical cure of postpartum pregnant women 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: |
陈通统 |
研究负责人: |
刘寿荣 |
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Applicant: |
Tongtong Chen |
Study leader: |
Songrong Liu |
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申请注册联系人电话: Applicant telephone: |
+86 178 1686 3740 |
研究负责人电话:
Study leader's |
+86 180 7293 0585 |
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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: |
1015439604@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
Lsr85463990@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: |
浙江省杭州市西湖区横埠街2号 |
研究负责人通讯地址: |
浙江省杭州市西湖区横埠街2号 |
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Applicant address: |
No. 2 Hengbu Street, Xihu District, Hangzhou, Zhejiang |
Study leader's address: |
No. 2 Hengbu Street, Xihu District, Hangzhou, Zhejiang |
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申请注册联系人邮政编码: Applicant postcode: |
310000 |
研究负责人邮政编码: Study leader's postcode: |
310000 |
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申请人所在单位: |
杭州市西溪医院 |
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Applicant's institution: |
Xixi Hospital of Hangzhou |
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研究负责人所在单位: |
杭州市西溪医院 |
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Affiliation of the Leader: |
Xixi Hospital of Hangzhou |
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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: |
杭西医伦审2024研第036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: |
杭州市西溪医院伦理委员会 |
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Name of the ethic committee: |
Xixi Hospital Ethics Committee of Hangzhou |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-05-20 00:00:00 | ||
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伦理委员会联系人: |
李兆翌 |
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Contact Name of the ethic committee: |
Zhaoyi Li |
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伦理委员会联系地址: |
浙江省杭州市西湖区横埠街2号 |
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Contact Address of the ethic committee: |
No. 2 Hengbu Street, Xihu District, Hangzhou, Zhejiang |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 571 8648 1703 |
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: |
杭州西溪医院 |
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Primary sponsor: |
Xixi Hospital of Hangzhou |
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研究实施负责(组长)单位地址: |
浙江省杭州市西湖区横埠街2号 |
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Primary sponsor's address: |
NO.2 hengbu street, xihu District |
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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: |
北京陈菊梅公益基金会 |
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Source(s) of funding: |
Beijing Chen Jumei Foundation |
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研究疾病: |
乙型病毒性肝炎 |
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Target disease: |
viral hepatitis type 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: |
最大限度实现乙肝孕妇产后HBsAg清除既产后乙肝临床治愈,改善肝病远期不良结局,最大程度降低肝硬化、肝癌的发生。 |
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Objectives of Study: |
Achieve clinical cure of hepatitis B after childbirth, improve the long-term adverse outcome of liver disease, minimize the occurrence of cirrhosis and liver cancer. |
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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) 孕期有严重合并症、产科并发症随访至产后未稳定(如妊娠合并糖尿病导致不稳定的糖尿病、子痫导致血压不稳定、严重甲状腺疾病未控制、产后大出血导致席汉综合征等; 2) 处于妊娠状态或近期有妊娠意愿; 3) 合并甲、丙、丁、戊肝、HIV感染等其他病毒感染性疾病; 4) 提示肝脏肿瘤:甲胎蛋白大于100ng/mL、或在试验前 3 个月内不能保持稳定和/或肝脏成像检查提示肝脏肿瘤; 5) 处于肝病失代偿期:肝脏组织学检查提示 G/S 评分大于 3 分、Child-Pugh ≥5 即符合以下一项:①血清白蛋白<3.5g/L;②凝血酶原时间延长≥3 秒;③血清胆红素>34umol/L;④有肝性脑病的病史;⑤有食管静脉曲张出血的病史;⑥腹水; 6) 有免疫介导的疾病史:如炎症性肠病、特发性血小板减少性紫癜、红斑狼疮、自身免疫性溶血性贫血、硬皮病、重度银屑病、类风湿性关节炎、自身免疫抗体水平异常升高; 7) 合并心、肺、肾、脑、血液等重要脏器严重疾病患者、或由其他证据表明为严重疾病或患有任何其他的疾病使得研究者认为患者不适合参加试验:如控制不稳定的糖尿病、高血压、甲状腺疾病、重度视网膜病变史或由其他证据表明为视网膜病变、重度癫痫史或当前正在使用抗癫痫药物治疗、 8) 入干扰素治疗组,还需要排除以下: ①严重的精神病史或爱丁堡试卷筛查有产后抑郁倾向;②肌酐高于正常值上限 1.5 倍者;③中性粒细胞计数<1.5×10^9 或血小板计数<90×10^9 ;④要求产后哺乳者;⑤对α-干扰素及其药物成分过敏者,研究者判断不适合应用α干扰素的患者(既往对于干扰素应用应答不佳);⑥受试者在进入本试验 4 周内接受过其他干扰素类药物的治疗;⑦器官移植史以及现存有功能性移植物(角膜或毛发移植除外) 9) 研究者评估认为不适合参加本研究的患者。 |
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Exclusion criteria: |
1) Severe comorbidities during pregnancy, obstetric complications persist during re-follow-up (such as unstable diabetes due to pregnancy and diabetes mellitus, unstable blood pressure due to eclampsia, uncontrolled severe thyroid disease, major postpartum haemorrhage resulting in Seehan syndrome, etc.); 2) Pregnant women or in the near future 3) Combination of A, C, D, hepatitis E, HIV infection and other viral infections; 4) liver tumors: alpha fetoprotein greater than 100 ng/mL, or failure to maintain stability and/or liver imaging within 3 months prior to the trial; 5) In the Liver Loss Period: Liver Histology Tips G/S Score Greater Than 3, Child-Pugh ≥5 Meets the Following One: 1 Serum albumin < 3.5g/L;2 prolonged thrombin duration ≥3 seconds; 3 serum bilirubin > 34umol/L; 4 has a history of hepatic encephalopathy; 5 have a history of esophageal varicose vein bleeding; 6 ascites; 6) Immuno-mediated diseases such as inflammatory bowel disease, idiopathic thrombocytopenic purpura, lupus erythematosus, autoimmune hemolytic anemia, scleroderma, severe psoriasis, rheumatoid arthritis, and abnormally elevated levels of autoimmune antibodies; 7) Patients with serious diseases such as heart, lung, kidney, brain, blood, and other important organs, or by other evidence of serious disease or any other disease, make the researchers believe that the patient is unfit to participate in the trial: unstable diabetes, hypertension, thyroid disease, history of severe retinopathy or other evidence of retinopathy, severe epilepsy or current use of antiepileptic drugs 8) In interferon therapy group, also need to exclude the following: ① severe psychiatric history or Edinburgh test paper screening has a tendency to postpartum depression;;②creatinine is 1.5 times higher than the normal limit;③neutrophil counts < 1.5 × 10^9 or platelet counts < 90 × 10^9 ;④require postpartum breastfeeding;⑤For those allergic to α-interferon and its pharmaceutical components, the researchers judged that it was not suitable for application α interferon patients (who did not respond well to interferon applications in the past);⑥Subjects entered this trial Received other interferon medications within 4 weeks;⑦History of organ transplantation and existing functional graft (except corneal or hair transplantation) 9) The researchers assessed that it was not suitable for the patients who participated in the study. |
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研究实施时间: Study execute time: |
从 From 2024-01-01 00:00:00至 To 2029-06-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-06-01 00:00:00 至 To 2026-05-01 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: |
正在进行 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): |
接诊患者的临床医生根据患者的个体情况和自身经验进行临床决策在推荐方案中选择,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。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Clinicians who receive patients make clinical decisions based on their individual circumstances and their own experience. The patients were classified into groups according to their baseline conditions and the options chosen, and entered into different cohorts for observation follow-up. |
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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: |
不公开/Private |
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盲法: |
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Blinding: |
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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): |
本研究分析的数据集可根据合理要求从通讯作者处获取。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The dataset analyzed in this study can be obtained from the corresponding authors according to reasonable requirements. |
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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: |
数据采集和管理由两部分组成,一为病例记录表,二为特定人员进行电子信息采集和管理。 |
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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 and management consist of two parts, one is the case record form, and the other is the electronic information collection and management by specific personnel. |
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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 |