|
注册号: Registration number: |
ChiCTR2500104166 |
|
最近更新日期: Date of Last Refreshed on: |
2025-06-12 09:08:56 |
|
注册时间: Date of Registration: |
2025-06-12 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
CyTOF检测白血病骨髓及外周血MRD效果对比 临床研究方案 |
|
Public title: |
Comparison of the effect of CyTOF in detecting MRD in bone marrow and peripheral blood of leukemia patients |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
CyTOF检测白血病骨髓及外周血MRD效果对比临床研究项目 |
|
Scientific title: |
Comparison of the effect of CyTOF in detecting MRD in bone marrow and peripheral blood of leukemia patients |
|
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: |
李美玲 |
研究负责人: |
胡建达,李美玲 |
|
Applicant: |
Meiling Li |
Study leader: |
Hu Jianda, Meiling Li |
|
申请注册联系人电话: Applicant telephone: |
+86 15880909409 |
研究负责人电话:
Study leader's |
+86 595 26650722 |
|
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: |
2189356143@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
973938301@qq.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: |
福建省泉州市丰泽区东海大街950号福建医科大学附属第二医院锦标楼六层血液内科 |
研究负责人通讯地址: |
福建省泉州市丰泽区中山北路34号 |
|
Applicant address: |
6th Floor, Jinbiao Building, Second Affiliated Hospital of Fujian Medical University, No. 950 Dongha |
Study leader's address: |
No. 34, Zhongshan North Road, Fengze District, Quanzhou City, Fujian Province |
|
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: |
福建医科大学附属第二医院 |
||
|
Applicant's institution: |
The Second Affiliated hospital of Fujian Medical University |
||
|
研究负责人所在单位: |
福建医科大学附属第二医院 |
||
|
Affiliation of the Leader: |
The Second Affiliated hospital of Fujian Medical University |
||
|
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: |
〔2025〕福医附二临研伦审第(011)号 |
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: |
福建医科大学附属第二医院临床研究与新技术新项目伦理委员会 |
||
|
Name of the ethic committee: |
The Ethics Committee For Clinical research, New technology And New Projects, The Second Affiliated Hospital Of Fujian Medical University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2025-03-10 00:00:00 | ||
|
伦理委员会联系人: |
徐美玲 |
||
|
Contact Name of the ethic committee: |
Xu Meiling |
||
|
伦理委员会联系地址: |
福建省泉州市丰泽区中山北路34号 |
||
|
Contact Address of the ethic committee: |
No. 34, Zhongshan North Road, Fengze District, Quanzhou City, Fujian Province |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 595 26655196 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
359410948@qq.com |
|
研究实施负责(组长)单位: |
福建医科大学附属第二医院 |
||||||||||||||||||||||
|
Primary sponsor: |
The Second Affiliated hospital of Fujian Medical University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
福建省泉州市丰泽区中山北路34号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 34, Zhongshan North Road, Fengze District, Quanzhou City, Fujian Province |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
自筹 |
||||||||||||||||||||||
|
Source(s) of funding: |
Self-funded |
||||||||||||||||||||||
|
研究疾病: |
急性髓系白血病 |
||||||||||||||||||||||
|
Target disease: |
Acute myeloid leukemia |
||||||||||||||||||||||
|
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: |
病例对照研究 |
||||||||||||||||||||||
|
Study design: |
Case-Control study |
||||||||||||||||||||||
|
研究目的: |
1. 主要目的: 建立一种统一、标准化、高精度的检测方法,通过CyTOF技术对比不同亚型白血病患者的免疫表型,以更早、更准确地预测疾病复发,辅助临床治疗决策。 2. 次要目的: (1) 明确不同白血病亚型患者的MRD(微小残留病)结果差异; 通过高精度检测分析不同亚型患者的MRD动态变化,为个体化临床干预(如强化治疗或停药)提供依据。 (2)验证外周血替代骨髓血的可行性; 比较骨髓血与外周血检测结果的一致性,探索侵入性更低的外周血检测方案,推动其在临床中的广泛应用。 |
||||||||||||||||||||||
|
Objectives of Study: |
1. Main purpose: A unified, standardized and high-precision detection method was established to compare the immunophenotypes of patients with different subtypes of leukemia through CyTOF technology, so as to predict disease recurrence earlier and more accurately, and assist clinical treatment decision-making. 2. Secondary Purpose: (1) To identify the differences in MRD (minimal residual disease) results among patients with different leukemia subtypes; The dynamic changes of MRD in patients with different subtypes were analyzed by high-precision detection to provide basis for individualized clinical intervention (such as intensive therapy or drug withdrawal). (2) To verify the feasibility of substituting peripheral blood for bone marrow blood; To compare the consistency of bone marrow blood and peripheral blood test results, explore a less invasive peripheral blood test scheme, and promote its wide application in clinic. |
||||||||||||||||||||||
|
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: |
1.年龄小于 14 岁的患者; 2.非初诊患者; 3.初诊 不为上述疾病患者; 4.诊断明确即放弃治疗患者。 5.健康人排除标准:恶性肿瘤及心肺功能衰竭影响到生命的的患者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Patients younger than 14 years of age; 2. Non-newly diagnosed patients; 3. Patients with the above diseases are not newly diagnosed; 4. When the diagnosis is clear, the treatment is abandoned. Exclusion criteria for healthy persons: patients with malignant tumors and cardiopulmonary failure affecting life. 5.Exclusion criteria for healthy individuals: Patients with malignant tumors or cardiopulmonary failure that is life-threatening; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2025-06-18 00:00:00至 To 2026-04-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-06-18 00:00:00 至 To 2025-12-30 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: |
尚未开始 Not yet recruiting |
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 |
否No |
|
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 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
|
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: |
病例记录表(CRF) |
|
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。 |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |