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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: |
ChiCTR2500100629 |
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最近更新日期: Date of Last Refreshed on: |
2025-04-11 16:12:20 |
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注册时间: Date of Registration: |
2025-04-11 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
异甘草酸镁预防恶性血液病患者新型抗肿瘤药物相关肝损伤的有效性和安全性:一项多中心、回顾性研究 |
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Public title: |
The efficacy and safety of magnesium isoglycyrrhizinate in preventing novel antitumor drug-related liver injury in patients with malignant hematological diseases: A multicenter, retrospective 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: |
异甘草酸镁预防恶性血液病患者新型抗肿瘤药物相关肝损伤的有效性和安全性:一项多中心、回顾性研究 |
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Scientific title: |
The efficacy and safety of magnesium isoglycyrrhizinate in preventing novel antitumor drug-related liver injury in patients with malignant hematological diseases: A multicenter, retrospective 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: |
梁晨 |
研究负责人: |
姜尔烈 |
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Applicant: |
Chen Liang |
Study leader: |
Erlie Jiang |
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申请注册联系人电话: Applicant telephone: |
+86 132 3303 4461 |
研究负责人电话: Study leader's telephone: |
+86 132 3303 4461 |
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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: |
danpingchu@outlook.com |
研究负责人电子邮件: Study leader's E-mail: |
jiangerlie@ihcams.ac.cn |
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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: |
天津市和平区南京路288号天津市静海区团泊大道28号 |
研究负责人通讯地址: |
天津市和平区南京路288号天津市静海区团泊大道28号 |
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Applicant address: |
No. 288, Nanjing Road, Heping District, Tianjin City, No. 28, Tuanbo Avenue, Jinghai District, Tianjin City |
Study leader's address: |
No. 288, Nanjing Road, Heping District, Tianjin City, No. 28, Tuanbo Avenue, Jinghai District, Tianjin City |
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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: |
中国医学科学院血液病医院(中国医学科学院血液学研究所) |
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Applicant's institution: |
China Academy of Medical Sciences Blood Disease Hospital (China Academy of Medical Sciences Hematology Institute) |
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研究负责人所在单位: |
中国医学科学院血液病医院(中国医学科学院血液学研究所) |
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Affiliation of the Leader: |
China Academy of Medical Sciences Blood Disease Hospital (China Academy of Medical Sciences Hematology Institute) |
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是否获伦理委员会批准: |
是/Yes |
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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: |
QTJC2024027-EC-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: |
中国医学科学院血液病医院(中国医学科学院血液学研究所)伦理审查委员会 |
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Name of the ethic committee: |
Ethics Committee of China Academy of Medical Sciences Blood Disease Hospital (China Academy of Medical Sciences Hematology Institute) |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-05-14 00:00:00 |
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伦理委员会联系人: |
肖志坚 |
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Contact Name of the ethic committee: |
Zhijian Xiao |
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伦理委员会联系地址: |
天津市和平区南京路288号 |
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Contact Address of the ethic committee: |
No. 288 Nanjing Road, Heping District, Tianjin |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 22 2390 9095 |
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: |
中国医学科学院血液病医院(中国医学科学院血液学研究所) |
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Primary sponsor: |
China Academy of Medical Sciences Blood Disease Hospital (China Academy of Medical Sciences Hematology Institute) |
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研究实施负责(组长)单位地址: |
天津市和平区南京路288号、天津市静海区团泊大道28号 |
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Primary sponsor's address: |
No. 288, Nanjing Road, Heping District, Tianjin City, No. 28, Tuanbo Avenue, Jinghai District, Tianjin City |
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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: |
自筹经费 |
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Source(s) of funding: |
Self-financing |
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Target disease: |
Hematologic Malignancy |
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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: |
本研究选取血液科恶性血液病患者作为研究对象,分析异甘草酸镁预防恶性血液病患者新型抗肿瘤药物相关肝损伤的结果,评价临床疗效和安全性,为其临床合理应用提供依据。 |
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Objectives of Study: |
In this study, patients with hematological malignancies in the Department of Hematology were selected as the study subjects to analyze the results of magnesium isoglycyrrhizinate in preventing liver injury associated with new anti-tumor drugs in patients with hematological malignancies, evaluate the clinical efficacy and safety, and provide the basis for its rational clinical application. |
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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)患者为恶性血液病患者(包括但不限于淋巴瘤、骨髓瘤、白血病); 2)年龄 ≥18周岁; 3)患者抗肿瘤治疗方案中至少包含1种新型抗肿瘤药物*; 4)使用含有异甘草酸镁预防肝损伤治疗时间为抗肿瘤治疗首个疗程当天或之前(异甘草酸镁剂量≥150mg/天,且用药持续时间≥5天); 5)患者使用异甘草酸镁预防前的TBiL≤1.0×ULN;ALT、AST≤1.0×ULN;ALP≤1.0×ULN; |
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Inclusion criteria |
1. Patients with hematological malignancies (including but not limited to lymphoma, myeloma, leukemia); 2. Age >= 18 years; 3. Patients with at least one new anti-tumor drug in the anti-tumor treatment regimen *; 4. The use of magnesium isoglycyrrhizinate to prevent liver injury treatment time is the first course of anti-tumor therapy on the day or before (magnesium isoglycyrrhizinate dose >= 150 mg/day, and medication duration >= 5 days); 5.TBiL <= 1.0 × ULN; ALT, AST <= 1.0 × ULN; ALP <= 1.0 × ULN before magnesium isoglycyrrhizinate prophylaxis; |
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排除标准: |
1)使用除异甘草酸镁外其他类型保肝药物的患者(如多烯磷脂酰胆碱、还原型谷胱甘肽及硫普罗宁等); 2)联合肝脏局部放疗的患者; 3)联合细胞免疫治疗*的患者; 4)乙肝或丙肝病毒处于复制状态,需要进行抗病毒治疗的患者; 5)缺少肝功能指标等关键临床资料信息,无法对抗肿瘤药物相关肝损伤的诊断做出临床判断的患者; *细胞免疫治疗包括细胞因子诱导的杀伤细胞疗法、树突状细胞疗法、DC+CIK细胞疗法、自然杀伤细胞疗法、DC~T细胞疗法等。 |
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Exclusion criteria: |
1.Patients using other types of hepatoprotective drugs except magnesium isoglycyrrhizinate (such as polyene phosphatidylcholine, reduced glutathione and tiopronin, etc.); 2. Patients with combined liver local radiotherapy; 3. Patients combined with cellular immunotherapy *; 4. Patients with hepatitis B or hepatitis C virus in a replicative state and requiring antiviral therapy; 5. Patients who lack key clinical data information such as liver function indicators and cannot make clinical judgment on the diagnosis of liver injury related to anti-tumor drugs; * Cellular immunotherapy includes cytokine-induced killer cell therapy, dendritic cell therapy, DC + CIK cell therapy, natural killer cell therapy, and DC ~ T cell therapy. |
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研究实施时间: Study execute time: |
从 From 2024-05-15 00:00:00至 To 2025-05-15 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-05-15 00:00:00 至 To 2025-05-15 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): |
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 |
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): |
研究结束后6个月,http://www.medresman.org.cn/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
6 months after the end of the study, http://www.medresman.org.cn/ |
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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: |
CRF表记录 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form |
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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 |