ChiCTR2000038294 版本V1.8 版本创建时间2020/12/13 12:17:29 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:

ChiCTR2000038294 

最近更新日期:

Date of Last Refreshed on:

2020-12-13 12:17:09 

注册时间:

Date of Registration:

2020-09-16 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

吴桢泉医师:请尽快在ResMan IPD 平台上传原始数据以完成补注册。 康柏西普与雷珠单抗单次玻璃体腔注射治疗ROP的多中心前瞻性随机对照研究

Public title:

Multi-central prospective randomized controlled trial of intravitreal injection of conbercept versus ranibizumab for retinopathy of prematurity

注册题目简写:

English Acronym:

研究课题的正式科学名称:

康柏西普与雷珠单抗单次玻璃体腔注射治疗ROP的多中心前瞻性随机对照研究

Scientific title:

Multi-central prospective randomized controlled trial of intravitreal injection of conbercept versus ranibizumab for retinopathy of prematurity

研究课题代号(代码):

Study subject ID:

深圳市科创委学科布局(项目编号:JCYJ20170817112542555)

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:

吴桢泉 

研究负责人:

张国明 

Applicant:

Wu Zhenquan 

Study leader:

Zhang Guoming 

申请注册联系人电话:

Applicant telephone:

+86 18250319927

研究负责人电话:

Study leader's telephone:

+86 13823509060

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:

wzq169cn@163.com

研究负责人电子邮件:

Study leader's E-mail:

13823509060@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:

广东省深圳市福田区泽田路18号

研究负责人通讯地址:

广东省深圳市福田区泽田路18号

Applicant address:

18 Zetian Road, Futian District, Shenzhen, Guangdong, China

Study leader's address:

18 Zetian Road, Futian District, Shenzhen, Guangdong, 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:

深圳市眼科医院

Applicant's institution:

Shenzhen Eye Hospital

研究负责人所在单位:

深圳市眼科医院

Affiliation of the Leader:

Shenzhen Eye Hospital

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:

20200628-07

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:

深圳市眼科医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Shenzhen Eye Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2020-06-28 00:00:00

伦理委员会联系人:

汪涛

Contact Name of the ethic committee:

Wang Tao

伦理委员会联系地址:

深圳市福田区泽田路18号

Contact Address of the ethic committee:

18 Zetian Road, Futian District, Shenzhen, Guangdong, 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:

深圳市眼科医院

Primary sponsor:

Shenzhen Eye Hospital

研究实施负责(组长)单位地址:

广东省深圳市福田区泽田路18号

Primary sponsor's address:

18 Zetian Road, Futian District, Shenzhen, Guangdong, 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):

广东

市(区县):

深圳

Country:

China

Province:

Guangdong

City:

Shenzhen

单位(医院):

深圳市眼科医院

具体地址:

福田区泽田路18号

Institution
hospital:

Shenzhen Eye Hospital

Address:

18 Zetian Road, Futian District

经费或物资来源:

深圳市科创委学科布局(项目编号:JCYJ20170817112542555)

Source(s) of funding:

The Project of Discipline Layout (No:JCYJ20170817112542555)

Target disease:

Retinopathy of prematurity

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:

比较康柏西普与诺适得单次玻璃体腔注射治疗APROP及1区或后极部2区ROP的6个月复发率。  

Objectives of Study:

To compare the recurrence rate and surgical complications of retinopathy of prematurity (ROP) between patients treated with intravitreal injection of conbercept (IVC) and ranibizumab (IVR) within 6 months.

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. APROP患儿;
2. 病变位于1区或后极部2区的ROP患儿;
3. 家属同意签署入组的知情同意书。

Inclusion criteria

1. Children with aprop;
2. Children with ROP whose lesions were located in zone 1 or zone 2 of posterior pole;
3. The family members agreed to sign the informed consent form.

排除标准:

1.患儿患有其他的眼部疾病;
2.既往曾接受抗VEGF、视网膜光凝术等及其他干预性治疗。

Exclusion criteria:

1. The child has other eye diseases;
2. Patients who have received anti VEGF, retinal photocoagulation and other intervention therapy in the past.

研究实施时间:

Study execute time:

From 2017-05-01 00:00:00 To 2019-02-28 00:00:00  

征募观察对象时间:

Recruiting time:

From 2017-05-01 00:00:00 To 2019-02-28 00:00:00  

干预措施:

Interventions:

组别:

1组

样本量:

30

Group:

Group 1

Sample size:

干预措施:

0.3mg/0.03ml 康柏西普单次玻璃体腔注射

干预措施代码:

Intervention:

intravitreal injection of conbercept (IVC) by 0.3mg/0.03ml

Intervention code:

组别:

2组

样本量:

30

Group:

Group 2

Sample size:

干预措施:

0.3mg/0.03ml 雷珠单抗单次玻璃体腔注射

干预措施代码:

Intervention:

intravitreal injection of ranibizumab (IVR) by 0.3mg/0.03ml

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东 

市(区县):

深圳 

Country:

China 

Province:

Guangdong 

City:

Shenzhen 

单位(医院):

深圳市眼科医院 

单位级别:

三级 

Institution
hospital:

Shenzhen Eye Hospital

Level of the institution:

Tertiary

测量指标:

Outcomes:

指标中文名:

复发率

指标类型:

主要指标

Outcome:

Recurrent rate

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

并发症发生率

指标类型:

次要指标

Outcome:

Complications rate

Type:

Secondary 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:

结束

/Completed

年龄范围:

Participant age:

最小 Min age 0 years
最大 Max age 0 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):

基于计算机随机方法,将入组患儿按1:1比例行康柏西普玻璃体腔注射治疗或雷珠单抗玻璃体腔注射治疗。

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

Based on a computer-generated randomization schedule, all eligible infants are randomly divided into 2 groups at a 1:1 proportion. Both eyes of each infant are then treated by IVC or IVR monotherapy.

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

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):

邮件抄送公开数据(13823509060@163.com)

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

Transmit data by E-mail(13823509060@163.com)

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:

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:

EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2020-09-16 06:05:21