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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: |
ChiCTR2400088604 |
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最近更新日期: Date of Last Refreshed on: |
2024-08-22 09:59:58 |
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注册时间: Date of Registration: |
2024-08-22 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: |
肿瘤患者治疗相关血液学毒性管理的多中心、真实世界研究 |
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Public title: |
the management of cancer treatment-related hematologic toxicity: a multicenter, real-world 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: |
肿瘤患者治疗相关血液学毒性管理的多中心、真实世界研究 |
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Scientific title: |
the management of cancer treatment-related hematologic toxicity: a multicenter, real-world 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: |
周建国 |
研究负责人: |
马虎 |
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Applicant: |
Jianguo Zhou |
Study leader: |
Hu Ma |
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申请注册联系人电话: Applicant telephone: |
+86 183 1154 3939 |
研究负责人电话: Study leader's telephone: |
+86 851 2759 6280 |
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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: |
jianguo.zhou@zmu.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
mahuab@163.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
https://www.zy2yy.cn/department_xbzlk/ |
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: |
新龙大道与新蒲大道交汇处 |
研究负责人通讯地址: |
区新龙大道与新蒲大道交汇处 |
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Applicant address: |
Intersection Of Xinlong And Xinpu Avenue |
Study leader's address: |
Intersection Of Xinlong And Xinpu Avenue |
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申请注册联系人邮政编码: Applicant postcode: |
563000 |
研究负责人邮政编码: Study leader's postcode: |
563000 |
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申请人所在单位: |
遵义医科大学第二附属医院 |
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Applicant's institution: |
The Second Affiliated Hospital of Zunyi Medical University |
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研究负责人所在单位: |
遵义医科大学第二附属医院 |
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Affiliation of the Leader: |
The Second Affiliated Hospital of Zunyi Medical University |
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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: |
KYLL-2024-042 |
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: |
遵义医科大学第二附属医院伦理审查委员会 |
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Name of the ethic committee: |
IRB of The Second Affiliated Hospital of Zunyi Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-05-15 00:00:00 |
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伦理委员会联系人: |
巩亮 |
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Contact Name of the ethic committee: |
Liang Gong |
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伦理委员会联系地址: |
新龙大道与新蒲大道交汇处 |
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Contact Address of the ethic committee: |
Intersection Of Xinlong And Xinpu Avenue |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 851 2759 6368 |
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: |
遵义医科大学第二附属医院 |
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Primary sponsor: |
The Second Affiliated Hospital of Zunyi Medical University |
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研究实施负责(组长)单位地址: |
新龙大道与新蒲大道交汇处 |
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Primary sponsor's address: |
Intersection Of Xinlong And Xinpu Avenue |
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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-funding |
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Target disease: |
Tumor |
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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: |
横断面 |
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Study design: |
Cross-sectional |
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研究目的: |
观察和评价在真实世界中,使用海曲泊帕乙醇胺片和/或硫培非格司亭等管理肿瘤患者治疗相关血液学毒性的有效性和安全性。 |
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Objectives of Study: |
To observe and evaluate the efficacy and safety of managing treatment-related hematologic toxicity in oncology patients in a real-world setting using, e.g., Hetropofol ethanolamine tablets and/or thiotepa fexofilgrastim. |
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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.前瞻性病例:患者签署知情同意书,自愿加入本研究;回顾性病例免签署知情同意书; 2.病理学或组织细胞学确诊罹患非髓性恶性肿瘤疾病; 3.年龄≥18岁,接受抗肿瘤治疗(化疗、放疗、靶免治疗等); 4.研究者评估需要对患者肿瘤治疗相关血液学毒性进行预防或治疗; |
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Inclusion criteria |
1. Prospective cases: patients signed an informed consent form to voluntarily enroll in the study; retrospective cases were exempted from signing the informed consent form; 2. Pathologically or cytologically confirmed diagnosis of non-myeloid malignant tumor; 3. Age ≥ 18 years, receiving anti-tumor therapy (chemotherapy, radiotherapy, target-free therapy, etc.); 4. investigator assessment of the need for prophylaxis or treatment of hematological toxicity associated with the patient's oncological treatment; |
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排除标准: |
1.怀孕期或哺乳期女性; 2.对硫培非格司亭、聚乙二醇重组人粒细胞刺激因子、TPO-RA及对大肠杆菌表达的其他制剂过敏者; 3.研究者判断其他不适合纳入研究的情况 |
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Exclusion criteria: |
1. Pregnant or lactating females; 2. allergy to thiotepa fexofilgrastim, polyethylene glycol recombinant human granulocyte stimulating factor, TPO-RA, and other agents expressed against Escherichia coli; 3. other conditions that, in the judgment of the investigator, make inclusion in the study inappropriate |
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研究实施时间: Study execute time: |
从 From 2024-09-08 00:00:00至 To 2025-10-14 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-09-08 00:00:00 至 To 2025-01-01 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: |
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: |
公开/Public |
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盲法: |
无 |
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Blinding: |
None |
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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 |
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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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: |
无 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
None |
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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 |