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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: |
ChiCTR1900022999 |
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最近更新日期: Date of Last Refreshed on: |
2019-05-06 18:00:45 |
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注册时间: Date of Registration: |
2019-05-06 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: |
中医药降低I期乙肝相关肝癌综合微创术后复发率的方案验证研究 |
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Public title: |
Validation study for the scheme of reducing the recurrence rate of hepatitis b-related hepatocellular carcinoma in stage I after comprehensive minimally Invasive surgery with traditional Chinese medicine. |
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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: |
中医药降低I期乙肝相关肝癌综合微创术后复发率的方案验证研究 |
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Scientific title: |
Validation study for the scheme of reducing the recurrence rate of hepatitis b-related hepatocellular carcinoma in stage I after comprehensive minimally Invasive surgery with traditional Chinese medicine. |
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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: |
赵晴 |
研究负责人: |
陈欣菊 |
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Applicant: |
Zhao Qing |
Study leader: |
Chen Xinju |
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申请注册联系人电话: Applicant telephone: |
+86 13721426916 |
研究负责人电话:
Study leader's |
+86 13700867158 |
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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: |
13721426916@163.com |
研究负责人电子邮件: Study leader's E-mail: |
chenxinju1215@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: |
河南省郑州市人民路19号 |
研究负责人通讯地址: |
河南省郑州市人民路19号 |
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Applicant address: |
19 Renmin Road, Zhengzhou, Henan, China |
Study leader's address: |
19 Renmin Road, Zhengzhou, Henan, China |
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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: |
河南中医药大学第一附属医院 |
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Applicant's institution: |
the First Affiliated Hospital of Henan University of TCM |
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研究负责人所在单位: |
河南中医药大学第一附属医院 |
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Affiliation of the Leader: |
the First Affiliated Hospital of Henan University of TCM |
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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: |
2018HL-079-01 |
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: |
河南中医学院第一附属医院伦理委员会 |
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Name of the ethic committee: |
1st Affilated Hospital of Henan College of Traditional Chinese Medicine Institutional Review Board |
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伦理委员会批准日期: Date of approved by ethic committee: |
2018-12-18 00:00:00 | ||
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伦理委员会联系人: |
王春芳 |
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Contact Name of the ethic committee: |
Wang Chunfang |
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伦理委员会联系地址: |
河南省郑州市人民路19号 |
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Contact Address of the ethic committee: |
19 Renmin Road, Zhengzhou, Henan, 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: |
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研究实施负责(组长)单位: |
河南中医药大学第一附属医院 |
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Primary sponsor: |
the First Affiliated Hospital of Henan University of TCM |
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研究实施负责(组长)单位地址: |
河南省郑州市人民路19号 |
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Primary sponsor's address: |
19 Renmin Road, Zhengzhou, Henan, 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: |
中央财政投入 |
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Source(s) of funding: |
central fiscal investment |
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研究疾病: |
I期乙肝相关肝癌 |
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Target disease: |
hepatitis b-related hepatocellular carcinoma in stage I |
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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: |
干预性研究 |
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Study type: |
Interventional 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: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
在前期研究基础之上,充分发挥中医药辨证论治优势,选择具有前期研究基础的有效中药制剂,通过科学的顶层方案设计和临床验证,获得具有确切疗效、能显著延缓I期乙肝相关肝癌疾病进展的综合治疗新方案。使I期乙肝相关肝癌综合微创术后2年复发率降低35%。 |
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Objectives of Study: |
On the basis of previous studies, give full play to the advantages of syndrome differentiation and treatment of traditional Chinese medicine, select effective traditional Chinese medicine preparations with the basis of previous studies, through scientific top-level program design and clinical validation, obtain a new comprehensive treatment program with definite curative effect and can significantly delay the progress of hepatitis B-related liver cancer disease in stage I. The recurrence rate of stage I hepatitis B-related hepatocellular carcinoma was reduced by 35% in 2 years after comprehensive minimally invasive surgery. |
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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)符合上述乙肝相关肝癌诊断标准的患者; |
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Inclusion criteria |
1) Patients who meet the diagnostic criteria of hepatitis B-related hepatocellular carcinoma; 2) Clinical stage I of primary hepatocellular carcinoma; 3) Administrated with comprehensive minimally invasive treatment witin 2 months. Images confirmed that there were no active lesions up to CR or measurable active lesions in vivo, which decreased by more than 80% compared with the original lesions (i.e., those with partial residual activity after comprehensive treatment, but could not be treated with minimally invasive treatment because of their special location). Child-Pugh grading A/B of liver function; 4) Aged 18-75 years, gender unlimited; 5) General condition was good, the Karnofsy score, 1 week before admission to the group, reaches 60 points; 6) Patients diagnosed as Zhengxu and Yuzhi syndrome by TCM; 7) Patients signed an informed consent to participate in the experimental study, and can ensure follow-up. |
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排除标准: |
1)以往(5年内)或同时患有其它未治愈的恶性肿瘤; |
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Exclusion criteria: |
1) In the past, within 5 years, or with other incurable malignant tumors at the same time; 2) Aminotransferase, AST or ALT, > 5 times normal value and/or total bilirubin significantly increased > 3 times normal value; 3) Patients with severe infection, fever, hemorrhagic tendency, refractory peritoneal effusion and stage III, IV hepatic encephalopathy; 4) Severe heart, lung and kidney diseases, cerebral hemorrhage. Patients with accidental or severe diabetic complications; 5) Pregnant or lactating women; patients with mental disorders; 6) Allergic constitutions or known allergies to the components of the drug; 7) Those who are participating in clinical trials of other drugs or receiving treatment with other traditional Chinese medicines; 8) Researchers believe that other causes are not suitable for clinical trials (e.g., combined with active alcoholic cirrhosis or autoimmune liver disease). |
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研究实施时间: Study execute time: |
从 From 2018-01-01 00:00:00至 To 2020-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2019-06-01 00:00:00 至 To 2019-09-30 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: |
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): |
本试验按照中心分层,由生物统计学家使用统计软件包产生两套随机用药编号。第一级为各病例号所对应的组别(A组、B组),第二级为2组所对应的处理(试验组和对照组)。随机编码表由中国中医科学院中医临床基础研究所评价中心完成,两级盲底分别单独密封,密封后由课题责任单位和统计人员保存。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
In this study, two sets of random drug numbers were generated by biostatisticians using statistical software packages. The first level is the group corresponding to each case number (group A, group B), and the second level is the treatment corresponding to the two groups (experimental group and control grou |
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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: |
双盲 |
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Blinding: |
Double blind |
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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): |
试验完成后6个月内公开;http://www.tcmcec.net/wcr |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Within six months after the trial complete;http://www.tcmcec.net/wcr |
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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: |
本次研究采用中国中医科学院中医临床基础医学研究所评价中心数据平台进行电子化数据管理,在试验启动之前对参加人员进行相关培训。数据管理员根据病例报告表构建e-CRF,并根据研究者提供的信息创建账号。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
In this study, the data platform of the evaluation center of the Institute of Clinical Basic Medicine of Chinese Academy of Traditional Chinese Medicine was used for electronic data management, and the participants were trained before the start of the experiment. Data managers construct e-CRF based on case reports and create accounts based on information provided by researchers. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |