硫唑嘌呤、吗替麦考酚酯、利妥昔单抗或静脉丙种球蛋白治疗儿童多相性MOG抗体相关疾病的前瞻性队列研究

注册号:

Registration number:

ChiCTR2100048742 

最近更新日期:

Date of Last Refreshed on:

2023-01-20 20:03:50 

注册时间:

Date of Registration:

2021-07-15 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

硫唑嘌呤、吗替麦考酚酯、利妥昔单抗或静脉丙种球蛋白治疗儿童多相性MOG抗体相关疾病的前瞻性队列研究

Public title:

Treatment responses of azathiopurine, mortimecofenate, rituximab and IVIg in children with relapsing myelin oligodendrocyte glycoprotein antibody–associated disease

注册题目简写:

English Acronym:

研究课题的正式科学名称:

硫唑嘌呤、吗替麦考酚酯、利妥昔单抗或静脉丙种球蛋白治疗儿童多相性MOG抗体相关疾病的前瞻性队列研究

Scientific title:

Treatment responses of azathiopurine, mortimecofenate, rituximab and IVIg in children with relapsing myelin oligodendrocyte glycoprotein antibody–associated disease

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:

常旭婷 

研究负责人:

吴晔 

Applicant:

Chang Xuting 

Study leader:

Wu Ye 

申请注册联系人电话:

Applicant telephone:

+86 18800159978

研究负责人电话:

Study leader's
telephone:

+86 13520756697

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:

changxt12@163.com

研究负责人电子邮件:

Study leader's E-mail:

dryewu@263.net

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:

北京市西城区西安门大街1号

研究负责人通讯地址:

北京市西城区西安门大街1号

Applicant address:

1 Xi'anmen Street, Xicheng District, Beijing

Study leader's address:

1 Xi'anmen Street, Xicheng District, Beijing

申请注册联系人邮政编码:

Applicant postcode:

100034

研究负责人邮政编码:

Study leader's postcode:

100034

申请人所在单位:

北京大学第一医院儿科

Applicant's institution:

Department of Pediatrics, Peking University First Hospital

研究负责人所在单位:

北京大学第一医院儿科

Affiliation of the Leader:

Department of Pediatrics, Peking University First Hospital

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2021科研089

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:

北京大学第一医院生物医学研究伦理委员会

Name of the ethic committee:

Ethics Committee of Peking University First Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2021-04-29 00:00:00

伦理委员会联系人:

汪科

Contact Name of the ethic committee:

Wang Ke

伦理委员会联系地址:

北京市西城区大红罗厂街6号

Contact Address of the ethic committee:

6 Luochang Street, Dahong, Xicheng District, Beijing

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 10 66119025

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:

北京大学第一医院儿科

Primary sponsor:

Department of Pediatrics, Peking University First Hospital

研究实施负责(组长)单位地址:

北京市西城区西安门大街1号

Primary sponsor's address:

1 Xi'anmen Street, Xicheng District, Beijing

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

北京

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

北京大学第一医院

具体地址:

西城区西安门大街1号

Institution
hospital:

Peking University First Hospital

Address:

1 Xi'anmen Street, Xicheng District

经费或物资来源:

Source(s) of funding:

No

研究疾病:

MOG-IgG相关疾病  

Target disease:

MOG-IgG associated disease

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:

上市后药物 

Study phase:

4

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

比较硫唑嘌呤、吗替麦考酚酯、利妥昔单抗和静脉丙种球蛋白治疗对儿童多相性MOG抗体相关疾病(MOGAD)预防复发治疗的有效性,从而为儿童MOGAD预防复发治疗的药物选择提供依据。  

Objectives of Study:

To compare the efficacy of azathioprine, mycophenolate mofetil, rituximab, and intravenous gamma globulin therapy for relapse prevention in children with multiphasic MOG antibody-associated disease (MOGAD), thereby providing a drug for children with MOGAD relapse prevention Choose to provide justification.

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.患有其他自身免疫性疾病(如干燥综合征、系统性红斑狼疮等);
2.合并自身免疫性脑炎相关抗体;
3.患有全身性细菌、病毒或真菌感染;
4.患恶性肿瘤或既往恶性肿瘤病史;
5.肝功能不全(ALT>3倍正常上限或AST>3倍正常上限);
6.肾功能不全(GFR<60ml/min);
7.血液系统疾病(Hb<60g/L,PLT<50x10^9/L,N<1x10^9/L , L<0.8x10^9/L);
8.不能接受MRI扫描的患者。

Exclusion criteria:

1. Suffering from other autoimmune diseases (such as Sj?gren's syndrome, systemic lupus erythematosus, etc.);
2. Combined with autoimmune encephalitis-related antibodies;
3. Suffer from systemic bacterial, viral or fungal infection;
4. Suffering from malignant tumor or previous history of malignant tumor;
5. Liver insufficiency (ALT > 3 times the upper limit of normal or AST > 3 times the upper limit of normal);
6. Renal insufficiency (GFR<60ml/min);
7. Hematological diseases (Hb<60g/L, PLT<50x10^9/L, N<1x10^9/L, L<0.8x10^9/L);
8. Patients who cannot undergo MRI scans.

研究实施时间:

Study execute time:

From 2021-08-01 00:00:00 To 2024-08-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2021-08-01 00:00:00 To 2024-08-01 00:00:00

干预措施:

Interventions:

组别:

硫唑嘌呤组

样本量:

30

Group:

azathiopurine group

Sample size:

干预措施:

硫唑嘌呤

干预措施代码:

Intervention:

azathiopurine

Intervention code:

组别:

利妥昔单抗组

样本量:

70

Group:

Rituximab group

Sample size:

干预措施:

利妥昔单抗

干预措施代码:

Intervention:

rituximab

Intervention code:

组别:

吗替麦考酚酯组

样本量:

70

Group:

mortimecofenate group

Sample size:

干预措施:

吗替麦考酚酯

干预措施代码:

Intervention:

mortimecofenate

Intervention code:

组别:

丙种球蛋白组

样本量:

30

Group:

gamma globulin group

Sample size:

干预措施:

丙种球蛋白

干预措施代码:

Intervention:

gamma globulin

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

北京大学第一医院 

单位级别:

三级甲等 

Institution
hospital:

Peking University First Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

2年复发率

指标类型:

主要指标

Outcome:

2 year relapse rate

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

组织:

Sample Name:

No

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

Note:

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age years
最大 Max age years

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):

Randomization Procedure (please state who generates the random number sequence and by what method):

No

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

盲法:

N/A

Blinding:

N/A

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

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):

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Not share

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

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-07-15 08:45:28