ChiCTR2100049467 版本V1.5 版本创建时间2022/03/09 13:30:43 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2100049467 

最近更新日期:

Date of Last Refreshed on:

2022-03-09 13:30:24 

注册时间:

Date of Registration:

2021-08-02 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

葡萄膜炎患者接种新型冠状病毒(COVID-19)疫苗的实效性随机对照试验

Public title:

A Pragmatic, Randomized Clinical Trial of Coronavirus (COVID-19) Vaccinations in Uveitis

注册题目简写:

English Acronym:

研究课题的正式科学名称:

葡萄膜炎患者接种新型冠状病毒(COVID-19)疫苗的实效性随机对照试验

Scientific title:

A Pragmatic, Randomized Clinical Trial of Coronavirus (COVID-19) Vaccinations in Uveitis

研究课题代号(代码):

Study subject ID:

CSTC, 2008CA5003

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:

杨培增 

研究负责人:

杨培增 

Applicant:

Yang Peizeng 

Study leader:

Yang Peizeng 

申请注册联系人电话:

Applicant telephone:

+86 13708349782

研究负责人电话:

Study leader's telephone:

+86 13708349782

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:

peizengycmu@126.com

研究负责人电子邮件:

Study leader's E-mail:

peizengycmu@126.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:

重庆市渝中区袁家岗友谊路1号

研究负责人通讯地址:

重庆市渝中区袁家岗友谊路1号

Applicant address:

1 Youyi Road, Yuzhong District, Chongqing, China

Study leader's address:

1 Youyi Road, Yuzhong District, Chongqing, China

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:

重庆医科大学附属第一医院

Applicant's institution:

the First Affiliated Hospital of Chongqing Medical University

研究负责人所在单位:

重庆医科大学附属第一医院

Affiliation of the Leader:

the First Affiliated Hospital of Chongqing Medical University

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

20214601

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:

重庆医科大学附属第一医院伦理委员会

Name of the ethic committee:

Ethics Committee of the First Affiliated Hospital of Chongqing Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2021-07-26 00:00:00

伦理委员会联系人:

严青

Contact Name of the ethic committee:

Yan Qing

伦理委员会联系地址:

重庆市渝中区袁家岗友谊路1号

Contact Address of the ethic committee:

1 Youyi Road, Yuanjiagang, Yuzhong District, Chongqing, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

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:

重庆医科大学附属第一医院

Primary sponsor:

The First Affiliated Hospital of Chongqing Medical University

研究实施负责(组长)单位地址:

重庆市渝中区袁家岗友谊路1号

Primary sponsor's address:

1 Youyi Road, Yuzhong District, Chongqing, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

重庆

市(区县):

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆医科大学附属第一医院

具体地址:

渝中区袁家岗友谊路1号

Institution
hospital:

The First Affiliated Hospital of Chongqing Medical University

Address:

1 Youyi Road, Yuzhong District

经费或物资来源:

重庆眼科重点实验室(CSTC,2008CA5003)

Source(s) of funding:

Chongqing Key Laboratory of Ophthalmology (CSTC, 2008CA5003)

Target disease:

uveitis

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

III期临床试验 

Study phase:

3

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要目的:检测葡萄膜炎患者立即接种COVID-19疫苗和延迟接种COVID-19疫苗之间的眼部和系统结果的差异。  

Objectives of Study:

Main purpose: to test the difference in ocular and systemic outcomes between prompt initiation of COVID-19 vaccination and deferred initiation of COVID-19 vaccination in patients with uveitis.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1.年龄≥18岁;
2.在筛查前尚未接种疫苗;
3.被诊断出任意眼睛有任何形式的葡萄膜炎;
4.非活动的疾病状态(满足以下所有条件):
(1)≦0.5+前房细胞;
(2)≦0.5+玻璃体混浊;
(3)无活动性炎症性脉络膜或视网膜血管病变。

Inclusion criteria

1. Age >= 18 years old;
2. Not vaccinated before screening;
3. Diagnosed with any form of uveitis in any eye;
4. Inactive disease state (all of the following are met):
(1)<=0.5+ anterior chamber cells;
(2)<=0.5+ vitreous opacity;
(3) No active inflammatory choroidal or retinal vascular disease.

排除标准:

1.葡萄膜炎完全缓解:在停止所有眼病治疗后3个月的无活动性疾病;
2.根据生产说明提供的任何已知疫苗禁忌症:
(1)有对任何疫苗成分过敏史的个体;
(2)体温超过38.5°C的个体;
(3)怀孕。
3.在研究者看来会因参与本研究而使受试者面临风险的任何其他情况。

Exclusion criteria:

1. Complete remission of uveitis: no active disease 3 months after discontinuation of all ophthalmic treatment;
2. Any known contraindications to the vaccine provided according to the manufacturing instructions:
(1) Individuals with a history of hypersensitivity to any vaccine component;
(2) Individuals whose body temperature exceeds 38.5 degree;
(3) Pregnancy.
3. Any other situation that, in the opinion of the investigator, would put the subject at risk due to participation in this study.

研究实施时间:

Study execute time:

From 2021-07-12 00:00:00 To 2022-07-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2021-08-02 00:00:00 To 2022-01-01 00:00:00  

干预措施:

Interventions:

组别:

试验组1

样本量:

657

Group:

Experimental group1

Sample size:

干预措施:

即时接种疫苗

干预措施代码:

Intervention:

prompt vaccination strategies

Intervention code:

组别:

试验组2

样本量:

657

Group:

Experimental group2

Sample size:

干预措施:

延迟接种疫苗

干预措施代码:

Intervention:

deferred vaccination strategies

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

重庆 

市(区县):

 

Country:

China 

Province:

Chongqing 

City:

 

单位(医院):

重庆医科大学附属第一医院 

单位级别:

三级甲等 

Institution
hospital:

The First Affiliated Hospital of Chongqing Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

葡萄膜炎恶化的时间

指标类型:

主要指标

Outcome:

time to worsening uveitis

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:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 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):

随机化清单将由统计学家使用电脑生成,并由指定的研究协调员妥善保存。该统计学家和指定的研究协调员将不参与试验的其他部分。

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

Randomization list will have been generated by a Statistician using a computer and will be properly kept by a Designated Study Coordinator.

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:

Blinding:

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

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):

联系项目负责人

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

contact project leader

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、电子采集和管理系统

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

CRF and an electronic data capture

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-08-02 08:46:49