ChiCTR1900023215 版本V1.0 版本创建时间2019/05/16 21:37:28 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:

ChiCTR1900023215 

最近更新日期:

Date of Last Refreshed on:

2019-05-16 21:35:19 

注册时间:

Date of Registration:

2019-05-16 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

硅油眼白内障患者人工晶体度数的选择

Public title:

Refractive outcomes of phacoemulsification after silicone oil filled using different lens calculation formulas

注册题目简写:

English Acronym:

研究课题的正式科学名称:

硅油眼白内障患者人工晶体度数的选择

Scientific title:

Refractive outcomes of phacoemulsification after silicone oil filled using different lens calculation formulas

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:

侯亚南 

研究负责人:

王一 

Applicant:

Yanan Hou 

Study leader:

Yi Wang 

申请注册联系人电话:

Applicant telephone:

+86 15155975725

研究负责人电话:

Study leader's
telephone:

+86 13808353062

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:

15155975725@163.com

研究负责人电子邮件:

Study leader's E-mail:

wangyieye@aliyun.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:

重庆市江北区华新街华唐路2号

研究负责人通讯地址:

重庆市江北区华新街华唐路2号

Applicant address:

2 Huatang Road, Jiangbei District, Chongqing, China

Study leader's address:

2 Huatang Road, Jiangbei 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:

重庆爱尔眼科医院

Applicant's institution:

Chongqing Aier EYE hospital

研究负责人所在单位:

重庆爱尔眼科医院

Affiliation of the Leader:

Chongqing Aier EYE hospital

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:

重庆爱尔眼科医院

Primary sponsor:

Chongqing Aier EYE hospital

研究实施负责(组长)单位地址:

重庆市江北区华新街华唐路2号

Primary sponsor's address:

2 Huatang Road, Jiangbei 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

市(区县):

Country:

China

Province:

Chongqing

City:

单位(医院):

重庆爱尔眼科医院

具体地址:

重庆市江北区华新街华唐路2号

Institution
hospital:

Chongqing Aier EYE hospital

Address:

2 Huatang Road, Jiangbei District, Chongqing, China

经费或物资来源:

重庆爱尔眼科医院

Source(s) of funding:

Chongqing Aier EYE hospital

研究疾病:

硅油眼并发性白内障  

Target disease:

complicated cataract after silicone oil filled

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:

通过前瞻性的设计来分析、比较不同的人工晶体计算公式对硅油眼患者并发性白内障人工晶体测算的准确性,为临床上硅油眼患者人工晶体公式选择做出指导。  

Objectives of Study:

The prospective design was used to analyze and compare the accuracy of different intraocular lens calculation formulas in the calculation of complicated cataract in patients with silicon-oil eyes, so as to provide guidance for the selection of intraocular lens formula in clinical patients with silicon-oil eyes.

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)硅油眼并发白内障患者,裂隙灯下检查角膜透明,无明显角膜水肿,矫正视力>0.1
2)有固视功能无弱视,患者可配合检查行IOL-master检查
3)眼底检查示视网膜贴附良好,无明显视网膜牵拉,增殖

Inclusion criteria

1) for the patients with silicon-oil eye complicated with cataract, the cornea was examined under the slit lamp, without obvious corneal edema, and the corrected visual acuity was >0.1;
2) patients with fixation function without amblyopia can be treated with ol-master examination;
3) fundus examination showed good retinal adhesion without obvious retinal stretch and proliferation.

排除标准:

1)之前同时行巩膜外垫压术
2)矫正视力<0.1
3)观察期间再次发生视网膜脱离
4)散瞳后悬韧带明显松弛或断裂。

Exclusion criteria:

1) performed scleral buckling at the same time before;
2) corrected vision acuity <0.1;
3) retinal detachment occurred again during observation
4) obvious relaxation or fracture of the suspensory ligament was observed after mydriasis;

研究实施时间:

Study execute time:

From 2019-05-20 00:00:00 To 2021-05-20 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-05-20 00:00:00 To 2021-05-20 00:00:00

干预措施:

Interventions:

组别:

Holladay1组

样本量:

20

Group:

Holladay1 Group

Sample size:

干预措施:

Holladay1公式测算

干预措施代码:

Intervention:

Holladay1 lens calculation

Intervention code:

组别:

Holladay2 组

样本量:

20

Group:

Holladay2 Group

Sample size:

干预措施:

Holladay2 公式测算

干预措施代码:

Intervention:

Holladay 2 lens calculation

Intervention code:

组别:

SRK/T 组

样本量:

20

Group:

SRK/T Group

Sample size:

干预措施:

SRK/T 公式测算

干预措施代码:

Intervention:

SRK/T lens calculation

Intervention code:

组别:

Barrett 组

样本量:

20

Group:

Barrett Group

Sample size:

干预措施:

Barrett 公式测算

干预措施代码:

Intervention:

Barrett lens calculation

Intervention code:

组别:

Hill-RBF 组

样本量:

20

Group:

Hill-RBF Group

Sample size:

干预措施:

Hill-RBF 公式测算

干预措施代码:

Intervention:

Hill-RBF lens calculation

Intervention code:

组别:

Haigis 组

样本量:

20

Group:

Haigis Group

Sample size:

干预措施:

Haigis 公式测算

干预措施代码:

Intervention:

Haigis lens calculation

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):

重庆爱尔眼科医院 

单位级别:

三级专科医院 

Institution
hospital:

Chongqing Aier EYE hospital

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

最佳矫正视力

指标类型:

主要指标

Outcome:

best corrected visual acuity

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

检影验光

指标类型:

主要指标

Outcome:

mydriatic optometry

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

电脑验光

指标类型:

主要指标

Outcome:

Computer optometry

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

iTrace验光

指标类型:

主要指标

Outcome:

iTrace optometry

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 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):

设计随机数字表,且通过纳入和排除标准的筛选的患者,依据患者抽取的数字序号进入相对应的组别中

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

Patients that are eligible to the inclusion and exclusion criteria are divided into different groups based on the random number they get.

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:

未说明

Blinding:

Not stated

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

是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):

2021-11-30 邮件

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

November 30, 2021,by e-mail

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:

病例记录表采集数据,ResMan软件管理数据

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

Data is collected by case record form, and is managed by ResMan software.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2019-05-16 21:35:19