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注册号: Registration number: |
ChiCTR2600123565 |
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最近更新日期: Date of Last Refreshed on: |
2026-04-28 09:38:31 |
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注册时间: Date of Registration: |
2026-04-28 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: |
不同治疗对药物性肝损伤患者预后的影响:一项前瞻性观察性研究 |
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Public title: |
Impact of Different Treatments on Prognosis in Patients with Drug-Induced Liver Injury: A Prospective Observational Study |
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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: |
不同治疗对药物性肝损伤患者预后的影响:一项前瞻性观察性研究 |
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Scientific title: |
Impact of Different Treatments on Prognosis in Patients with Drug-Induced Liver Injury: A Prospective Observational Study |
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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: |
景婧 |
研究负责人: |
陆荫英 |
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Applicant: |
Jing Jing |
Study leader: |
Lu Yinying |
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申请注册联系人电话: Applicant telephone: |
+86 138 1045 4271 |
研究负责人电话:
Study leader's |
+86 133 0125 6799 |
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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: |
meg-forever@163.com |
研究负责人电子邮件: Study leader's E-mail: |
meg-forever@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
中国人民解放军总医院第五医学中心 |
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: |
中国北京市丰台区西四环中路100号 |
研究负责人通讯地址: |
中国北京市丰台区西四环中路100号 |
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Applicant address: |
100 West Fourth Ring Middle Road, Fengtai District, Beijing, China |
Study leader's address: |
100 West Fourth Ring Middle Road, Fengtai District, Beijing, 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: |
中国人民解放军总医院第五医学中心 |
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Applicant's institution: |
Fifth Medical Center, Chinese PLA General Hospital |
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研究负责人所在单位: |
中国人民解放军总医院第五医学中心 |
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Affiliation of the Leader: |
Fifth Medical Center, Chinese PLA General 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: |
KY-2025-8-164-1 |
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: |
中国人民解放军总医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Chinese PLA General Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-08-10 00:00:00 | ||
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伦理委员会联系人: |
张昕洁 |
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Contact Name of the ethic committee: |
Zhang Xinjie |
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伦理委员会联系地址: |
中国北京市丰台区东大街8号 |
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Contact Address of the ethic committee: |
8 East Street, Fengtai District, Beijing, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 6694 7798 |
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: |
中国人民解放军总医院第五医学中心 |
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Primary sponsor: |
Fifth Medical Center, Chinese PLA General Hospital |
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研究实施负责(组长)单位地址: |
中国北京市丰台区西四环中路100号 |
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Primary sponsor's address: |
100 West Fourth Ring Middle Road, Fengtai District, Beijing, 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: |
自筹 |
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Source(s) of funding: |
Self-funded |
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研究疾病: |
药物性肝损伤 |
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Target disease: |
Drug-induced liver injury, DILI |
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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: |
1. 观察真实世界队列中DILI患者接受不同治疗方案的成本-效果比; 2. 观察真实世界队列中不同治疗方案对DILI患者的远期影响。 |
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Objectives of Study: |
1. To observe the cost-effectiveness ratio of different treatment regimens for patients with DILI in a real-world cohort; 2. To observe the long-term effects of different treatment regimens on DILI patients in a real-world cohort. |
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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. 年龄18岁以下; 2. 非药物引起的各种类型的肝损伤患者; 3. 本次肝生化异常是由其他原因(如病毒性肝炎、酒精性肝病、代谢相关脂肪性肝病、自身免疫性肝病等)引起; 4. 重度以上或危及生命的心、肺、脑、肾、胃肠道及全身系统疾病者; 5. 患者无能力表达自己的主诉,如精神疾病等; 6. 依从性差不能合作者; 7. 孕妇、哺乳期妇女; 8. 3个月内参加其他临床试验者; 9. 研究者认为有任何不适合入选的情况。 |
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Exclusion criteria: |
1. Age under 18 years; 2. Patients with liver injury not caused by drugs; 3. Current liver biochemical abnormalities caused by other etiologies (e.g., viral hepatitis, alcoholic liver disease, metabolic dysfunction-associated fatty liver disease, autoimmune liver disease, etc.); 4. Severe or life-threatening diseases of the heart, lungs, brain, kidneys, gastrointestinal tract, or systemic conditions; 5. Patients unable to express their chief complaints, such as those with mental disorders; 6. Patients with poor compliance who are unable to cooperate; 7. Pregnant or lactating women; 8. Participation in other clinical trials within the past 3 months; 9. Any other conditions deemed inappropriate for inclusion by the investigator. |
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研究实施时间: Study execute time: |
从 From 2025-08-10 00:00:00至 To 2028-11-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-05-01 00:00:00 至 To 2028-11-30 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: |
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): |
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: |
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): |
不共享原始数据 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
No share IPD. |
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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: |
记录病例记录表,搭建管理电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
A standard data collection and management system include a CRF and an electronic data. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |