ChiCTR2600125085 版本V1.0 版本创建时间2026/05/21 10:29:33 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:

ChiCTR2600125085 

最近更新日期:

Date of Last Refreshed on:

2026-05-21 10:29:11 

注册时间:

Date of Registration:

2026-05-21 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

圆锥角膜家系的遗传学多中心研究

Public title:

Multicenter Genetic Study of Keratoconus Families?

注册题目简写:

English Acronym:

研究课题的正式科学名称:

圆锥角膜家系的遗传学多中心研究

Scientific title:

Multicenter Genetic Study of Keratoconus Families?

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:

李兴勇 

研究负责人:

陈世豪 

Applicant:

Xingyong Li 

Study leader:

Shihao Chen 

申请注册联系人电话:

Applicant telephone:

+86 577 88068862

研究负责人电话:

Study leader's
telephone:

+86 577 88068862

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:

lixy@eye.ac.cn

研究负责人电子邮件:

Study leader's E-mail:

csh@eye.ac.cn

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:

温州市学院西路270号温州医科大学附属眼视光医院屈光手术中心

研究负责人通讯地址:

浙江省温州市学院西路270号

Applicant address:

270, West Xueyuan Road, Refractive Surgery Center, Eye Hospital, Wenzhou Medical University, Wenzhou

Study leader's address:

270 West Xueyuan Road, Wenzhou, Zhejiang, 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:

温州医科大学附属眼视光医院

Applicant's institution:

Eye Hospital, Wenzhou Medical University

研究负责人所在单位:

温州医科大学附属眼视光医院

Affiliation of the Leader:

Eye Hospital, Wenzhou Medical University

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:

温医大眼视光伦审2026研第104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:

温州医科大学附属眼视光医院伦理委员会

Name of the ethic committee:

Ethics committee of Eye Hospital of Wenzhou Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2026-04-10 00:00:00

伦理委员会联系人:

谷佩秋

Contact Name of the ethic committee:

Gu Peiqiu

伦理委员会联系地址:

浙江省温州市学院西路270号

Contact Address of the ethic committee:

270 West Xueyuan Road, Wenzhou, Zhejiang, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 577 88075582

伦理委员会联系人邮箱:

Contact email of the ethic committee:

gupeiqiu@126.com

研究实施负责(组长)单位:

温州医科大学附属眼视光医院

Primary sponsor:

Eye Hospital, Wenzhou Medical University

研究实施负责(组长)单位地址:

浙江省温州市学院西路270号

Primary sponsor's address:

270 West Xueyuan Road, Wenzhou, Zhejiang, 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):

浙江省

市(区县):

Country:

China

Province:

Zhejiang

City:

单位(医院):

温州医科大学附属眼视光医院

具体地址:

浙江省温州市学院西路270号

Institution
hospital:

Eye Hospital, Wenzhou Medical University

Address:

270 West Xueyuan Road, Wenzhou, Zhejiang, China

经费或物资来源:

温州医科大学附属眼视光医院1010计划项目

Source(s) of funding:

1010 Program Project of Eye Hospital, Wenzhou Medical University

研究疾病:

圆锥角膜  

Target disease:

keratoconus

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:

本项目将通过开展多中心研究,基于遗传测序探索圆锥角膜的致病基因和位点。  

Objectives of Study:

This project will conduct a multicenter study to explore the pathogenic genes and loci of keratoconus based on genetic sequencing.

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.先证者有至少一只眼睛被确诊为原发性圆锥角膜; 2.家系至少包括先证者及其父母3人参与; 3.家系参与成员同意参与此项研究。

Inclusion criteria

1. The proband must have at least one eye diagnosed with primary keratoconus; 2. The family pedigree must include at least the proband and both parents (a minimum of 3 participants); 3. All participating family members have agreed to participate in this study.

排除标准:

1.先证者诊断为非原发性圆锥角膜,例如继发性圆锥角膜; 2.家系参与人员数量不足,无法达到研究要求; 3.家系参与者的临床数据或生物样本缺失,无法达到研究要求。

Exclusion criteria:

1. The proband is diagnosed with non-primary keratoconus, e.g., secondary keratoconus; 2. The number of participating family members is insufficient to meet the study requirements; 3. The clinical data or biological samples from the family participants are missing, failing to meet the study requirements.

研究实施时间:

Study execute time:

From 2026-01-01 00:00:00 To 2030-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2026-06-01 00:00:00 To 2030-12-31 00:00:00

干预措施:

Interventions:

组别:

病例组

样本量:

2400

Group:

Case Group

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江省 

市(区县):

 

Country:

China

Province:

Zhejiang

City:

单位(医院):

温州医科大学附属眼视光医院 

单位级别:

三级甲等 

Institution
hospital:

Eye Hospital, Wenzhou Medical University

Level of the institution:

Tertiary A

国家:

希腊

省(直辖市):

Heraklion 

市(区县):

 

Country:

Greece

Province:

Heraklion

City:

单位(医院):

Emmetropia Mediterranean Eye Institute 

单位级别:

无 N/A 

Institution
hospital:

Emmetropia Mediterranean Eye Institute

Level of the institution:

N/A

国家:

约旦

省(直辖市):

Amman 

市(区县):

 

Country:

Jordan

Province:

Amman

City:

单位(医院):

School of Medicine, The University of Jordan 

单位级别:

无 N/A 

Institution
hospital:

School of Medicine, The University of Jordan

Level of the institution:

N/A

测量指标:

Outcomes:

指标中文名:

基因突变

指标类型:

主要指标

Outcome:

genetic locus

Type:

Primary indicator

测量时间点:

测量方法:

全外显子测序

Measure time point of outcome:

Measure method:

Whole Exome Sequencing

指标中文名:

视力、角膜体征、角膜地形图、角膜生物力学

指标类型:

主要指标

Outcome:

corneal signs, corneal topography, corneal biomechanics

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:

外周静脉血

组织:

Sample Name:

Peripheral Venous Blood

Tissue:

人体标本去向

使用后保存  

说明

Fate of sample:

Preservation after use  

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 0 years
最大 Max age 45 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):

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:

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):

不适用

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

Not Applicable

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:

所有数据将于入组时采集,数据采集后将进行数据脱敏处理。数据将由专人进行管理。

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

All data will be collected at the time of enrollment. After data collection, the data will undergo anonymization processing. The data will be managed by designated personnel.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2026-05-21 10:29:11