|
注册号: Registration number: |
ChiCTR2500112530 |
|
最近更新日期: Date of Last Refreshed on: |
2025-11-17 08:24:18 |
|
注册时间: Date of Registration: |
2025-11-17 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
流式细胞术外周血淋巴细胞亚群关键指标质量目标的建立和验证研究 |
|
Public title: |
Establishment and validation of key index quality targets of peripheral blood lymphocyte subsets by flow cytometry |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
流式细胞术外周血淋巴细胞亚群关键指标质量目标的建立和验证研究 |
|
Scientific title: |
Establishment and validation of key index quality targets of peripheral blood lymphocyte subsets by flow cytometry |
|
研究课题代号(代码): Study subject ID: |
|
|
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: |
|
申请注册联系人: |
肖琳 |
研究负责人: |
肖琳 |
|
Applicant: |
Xiao Lin |
Study leader: |
Xiao Lin |
|
申请注册联系人电话: Applicant telephone: |
+86 10 8778 7503 |
研究负责人电话:
Study leader's |
+86 10 8778 7503 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
xiaolin5022@sina.com |
研究负责人电子邮件: Study leader's E-mail: |
xiaolin5022@sina.com |
|
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): |
||
|
申请注册联系人通讯地址: |
北京市朝阳区潘家园南里17号 |
研究负责人通讯地址: |
北京市朝阳区潘家园南里17号 |
|
Applicant address: |
No. 17, Panjiayuan Nanli, Chaoyang District, Beijing |
Study leader's address: |
No. 17, Panjiayuan Nanli, Chaoyang District, Beijing |
|
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: |
||
|
申请人所在单位: |
国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院检验科 |
||
|
Applicant's institution: |
Department of Clinical Laboratory, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College |
||
|
研究负责人所在单位: |
国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院检验科 |
||
|
Affiliation of the Leader: |
Department of Clinical Laboratory, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
24/115-4395 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
中国医学科学院肿瘤医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of Cancer Hospital, Chinese Academy of Medical Sciences |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2024-03-01 00:00:00 | ||
|
伦理委员会联系人: |
徐震纲 |
||
|
Contact Name of the ethic committee: |
Xu Zhengang |
||
|
伦理委员会联系地址: |
北京市朝阳区潘家园南里17号 |
||
|
Contact Address of the ethic committee: |
No. 17, Panjiayuan Nanli, Chaoyang District, Beijing |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 8778 8495 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
|
|
研究实施负责(组长)单位: |
中国医学科学院肿瘤医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
北京市朝阳区潘家园南里17号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 17, Panjiayuan Nanli, Chaoyang District, Beijing |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
北京市自然科学基金 |
||||||||||||||||||||||
|
Source(s) of funding: |
Beijing Natural Science Foundation |
||||||||||||||||||||||
|
研究疾病: |
外周血淋巴细胞亚群 |
||||||||||||||||||||||
|
Target disease: |
Peripheral blood lymphocyte subsets |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
横断面 |
||||||||||||||||||||||
|
Study design: |
Cross-sectional |
||||||||||||||||||||||
|
研究目的: |
本研究旨在通过多中心联合验证外周血淋巴细胞流式检测的关键指标差异,验证评估实际可接纳范围,建立质量目标和标准化流程,为淋巴细胞亚群检测性能验证提供参考依据,辅助行业标准的制定,填补国际领域的空白。 |
||||||||||||||||||||||
|
Objectives of Study: |
This study aims to verify the differences in key indicators of peripheral blood lymphocyte flow cytometry through multi-center joint verification, verify the actual acceptability range of evaluation, establish quality objectives and standardized processes, provide a reference for the verification of lymphocyte subset detection performance, assist in the formulation of industry standards, and fill the gap in the international field. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
确诊血液肿瘤的患者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
Patients with a confirmed hematological tumor. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-04-01 00:00:00至 To 2024-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-04-15 00:00:00 至 To 2024-10-15 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
结束 /Completed |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
||||||||
|
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 |
|
盲法: |
无 |
|
Blinding: |
None |
|
是否共享原始数据: IPD sharing |
是Yes |
|
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,通过ResMan(www.medresman.org.cn)方式共享 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the end of the study, it was shared by ResMan (www.medresman.org.cn). |
|
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;EDC |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF;EDC |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |