ChiCTR2100050163 版本V1.1 版本创建时间2022/04/24 07:25:00 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:

ChiCTR2100050163 

最近更新日期:

Date of Last Refreshed on:

2022-04-03 15:52:39 

注册时间:

Date of Registration:

2021-08-19 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

请于伦理委员会批准后才开始征募参试者,并与我们联系上传伦理批件。 高度近视黄斑劈裂的优化手术策略研究

Public title:

Optimization of surgical strategy for myopic foveoschisis

注册题目简写:

English Acronym:

研究课题的正式科学名称:

高度近视黄斑劈裂的优化手术策略研究

Scientific title:

Optimization of surgical strategy for myopic foveoschisis

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:

林威 

研究负责人:

魏勇 

Applicant:

Lin Wei 

Study leader:

Wei Yong 

申请注册联系人电话:

Applicant telephone:

+86 13587560390

研究负责人电话:

Study leader's
telephone:

+86 15057551266

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:

linweiysg@163.com

研究负责人电子邮件:

Study leader's E-mail:

weiyongdoctor@163.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:

浙江省温州市鹿城区学院西路270号

研究负责人通讯地址:

浙江省温州市鹿城区学院西路270号

Applicant address:

270 Xueyuan Road West, Lucheng District, Wenzhou, Zhejiang, China

Study leader's address:

270 Xueyuan Road West, Lucheng District, 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:

The Eye Hospital of 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:

The Eye Hospital of Wenzhou Medical University

是否获伦理委员会批准:

Approved by ethic committee:

No

伦理委员会批件文号:

Approved No. of ethic committee:

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

Name of the ethic committee:

伦理委员会批准日期:

Date of approved by ethic committee:

2013-08-26 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

温州医科大学附属眼视光医院

Primary sponsor:

The Eye Hospital of Wenzhou Medical University

研究实施负责(组长)单位地址:

浙江省温州市鹿城区学院西路270号

Primary sponsor's address:

270 Xueyuan Road West, Lucheng District, 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

市(区县):

温州

Country:

China

Province:

Zhejiang

City:

Wenzhou

单位(医院):

温州医科大学附属眼视光医院

具体地址:

鹿城区学院西路270号

Institution
hospital:

The Eye Hospital of Wenzhou Medical University

Address:

270 Xueyuan Road West, Lucheng District

经费或物资来源:

温州医科大学附属眼视光医院科研启动基金

Source(s) of funding:

Supporting Funds of The Eye Hospital of Wenzhou Medical University

研究疾病:

高度近视黄斑劈裂  

Target disease:

myopic foveoschisis

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

在近视性黄斑劈裂的玻璃体视网膜手术中,比较“C”型内界膜撕除+内界膜翻转覆盖与保留黄斑中心凹的内界膜撕除术,术后视觉质量和解剖结构的变化。  

Objectives of Study:

In vitreoretinal surgery for myopic foveoschisis, the changes in postoperative visual quality and anatomical structure were compared between "C" type inner limiting membrane avulsion + inverted cover of inner limiting membrane and inner limiting membrane avulsion retaining macular fovea.

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.高度近视眼(屈光度>-6.0D,眼轴>26.5mm)合并黄斑劈裂,存在近视性黄斑病变(分类0-分类1),近期有明显的视力下降或视物变形;
2.近视性黄斑劈裂发生黄斑内层或外层裂孔,或发生黄斑中心凹脱离(T3),
3.患者年龄≥18岁;
4,能够且愿意加入临床试验。

Inclusion criteria

1. High myopia (diopter > -6.0d, axis > 26.5mm) with macular cleavage, myopic macular disease (classification 0- classification 1), and recent significant visual acuity loss or distortion;
2. Myopic macular cleavage with inner or outer macular holes, or macular fovea detachment (T3);
3. Patients aged >=18 years;
4. Able and willing to participate in clinical trials.

排除标准:

1.近视性黄斑劈裂,存在近视性黄斑病变(合并“Plus”损害);
2.合并近视性黄斑裂孔或黄斑裂孔性视网膜脱离;
3.屈光介质混浊严重影响视力(包括严重的白内障,角膜白斑等);
4.既往接受过玻璃体视网膜手术或者后巩膜加固术;
5.预期不能在指定临床实验中心随访者;
6.存在神经系统或者精神类疾病不能配合检查者。

Exclusion criteria:

1. Myopic macular cleavage, myopic macular disease (combined with "Plus" damage);
2. myopic macular hole or macular hole retinal detachment;
3. Refractive media opacity seriously affects vision (including severe cataract, corneal leukoplakia, etc);
4. previous vitreoretinal surgery or posterior scleral reinforcement;
5. Visitors are not expected to be in the designated clinical trial center;
6. Having neurological or psychiatric diseases and unable to cooperate with the examination;

研究实施时间:

Study execute time:

From 2021-09-01 00:00:00 To 2024-08-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2021-09-01 00:00:00 To 2024-08-01 00:00:00

干预措施:

Interventions:

组别:

内界膜翻转覆盖组

样本量:

17

Group:

The inner limiting membrane inverted covering group

Sample size:

干预措施:

内界膜翻转覆盖

干预措施代码:

Intervention:

The inner limiting membrane is inverted covering

Intervention code:

组别:

中心凹内界膜保留组

样本量:

17

Group:

The endofovea inner limting membrane retained group

Sample size:

干预措施:

保留中心凹内界膜

干预措施代码:

Intervention:

Retained the endofovea inner limting membrane

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江 

市(区县):

温州 

Country:

China

Province:

Zhejiang

City:

Wenzhou

单位(医院):

温州医科大学附属眼视光医院 

单位级别:

三甲 

Institution
hospital:

The Eye Hospital of Wenzhou Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

黄斑劈裂改善情况

指标类型:

主要指标

Outcome:

improvement of myopic foveoschisis

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:

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):

随机数字表

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

random number table

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

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):

还未公开,未定

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

undecided

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

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

Case Record Form, CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-08-19 09:14:50