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注册号: Registration number: |
ChiCTR2300076702 |
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最近更新日期: Date of Last Refreshed on: |
2024-04-18 16:23:12 |
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注册时间: Date of Registration: |
2023-10-16 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: |
L-CBA法检测MOG-IgG的临床应用价值分析:多中心前瞻性临床研究 |
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Public title: |
Clinical application value analysis of L-CBA method for detecting MOG-IgG: a multicenter prospective clinical 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: |
L-CBA法检测MOG-IgG的临床应用价值分析:多中心前瞻性临床研究 |
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Scientific title: |
Clinical application value analysis of L-CBA method for detecting MOG-IgG: a multicenter prospective clinical 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: |
周勇 |
研究负责人: |
孙丹 |
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Applicant: |
Zhou Yong |
Study leader: |
Sun dan |
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申请注册联系人电话: Applicant telephone: |
+86 185 0271 1686 |
研究负责人电话:
Study leader's |
+86 139 7161 6910 |
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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: |
zhouyong8@kindstar.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
bloveriver@163.com |
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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: |
湖北省武汉市东湖新技术开发区豹澥街道高科园三路9号武汉光谷精准医疗产业基地2.1期10号楼302号(自贸区武汉片区) |
研究负责人通讯地址: |
湖北省武汉市江岸区香港路100号 |
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Applicant address: |
302, Building 10, Phase 2.1, Wuhan Optics Valley Precision Medical Industrial Base, 9 Gaokeyuan 3rd Road, Baoxie Street, Wuhan East Lake New Technology Development Zone (Pilot Free Trace Zone Wuhan Area), Wuhan, Hubei |
Study leader's address: |
100 Hongkong Road, Jiang'an District, Wuhan, Hubei, 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: |
迈诺(武汉)医学生物科技有限公司 |
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Applicant's institution: |
Maino (Wuhan) Medical Biotechnology Co., Ltd |
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研究负责人所在单位: |
华中科技大学同济医学院武汉儿童医院 |
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Affiliation of the Leader: |
Wuhan Children's Hospital of Tongji Medical College, Huazhong University of Science and Technology |
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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: |
2023R041-E02 |
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: |
武汉儿童医院(武汉市妇幼保健院)医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital) |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-08-12 00:00:00 | ||
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伦理委员会联系人: |
肖晗 |
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Contact Name of the ethic committee: |
Han Xiao |
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伦理委员会联系地址: |
湖北省武汉市江岸区香港路100号 |
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Contact Address of the ethic committee: |
100 Hongkong Road, Jiang'an District, Wuhan, Hubei, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 27 8243 8516 |
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: |
华中科技大学同济医学院附属武汉儿童医院 |
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Primary sponsor: |
Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science & Technology |
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研究实施负责(组长)单位地址: |
湖北省武汉市江岸区香港路100号 |
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Primary sponsor's address: |
100 Hongkong Road, Jiang'an District, Wuhan, Hubei, 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: |
医院自筹 |
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Source(s) of funding: |
Self funded |
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研究疾病: |
抗髓鞘少突胶质细胞糖蛋白免疫球蛋白G抗体相关疾病 |
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Target disease: |
anti-myelin oligodendrocyte glycoprotein-IgG associated disorders |
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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: |
比较F-CBA和L-CBA法检测MOG-IgG抗体的特异性及灵敏度;建立适合中国人群的MOG-IgG阳性滴度阈值;探究抗体滴度在治疗预后中的意义。 |
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Objectives of Study: |
To compare the specificity and sensitivity of F-CBA and L-CBA methods for detecting MOG-IgG antibodies; To establish a MOG-IgG positive titer threshold suitable for the Chinese population; To explore the significance of antibody titers in treatment prognosis. |
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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.首次发病年龄>18岁; 2.不符合各组的入组标准; 3.患者依从性差,就诊资料不全。 |
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Exclusion criteria: |
1. The age of first onset is greater than 18 years old; 2. Not meeting the inclusion criteria for each group; 3. Patients have poor compliance and incomplete medical information. |
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研究实施时间: Study execute time: |
从 From 2023-09-01 00:00:00至 To 2025-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-10-20 00:00:00 至 To 2024-12-31 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): |
本研究不涉及随机。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This study does not involve random. |
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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 |
是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): |
原始数据不共享。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Raw data is not shared. |
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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: |
数据采集合管理均通过病例注册登记平台进行。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection and management are carried out through the case registration platform. |
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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 |