ChiCTR2300070802 版本V1.0 版本创建时间2023/04/23 17:59:34 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:

ChiCTR2300070802 

最近更新日期:

Date of Last Refreshed on:

2023-04-23 17:59:20 

注册时间:

Date of Registration:

2023-04-23 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

区域折射景深延长型人工晶状体植入术后的视觉效果观察

Public title:

Observation of visual effects after regional refraction depth-of-field extension intraocular lens implantation

注册题目简写:

English Acronym:

研究课题的正式科学名称:

区域折射景深延长型人工晶状体植入术后的视觉效果观察

Scientific title:

Observation of visual effects after regional refraction depth-of-field extension intraocular lens implantation

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:

唐凯莉 

研究负责人:

张劲松 

Applicant:

Tang Kaili 

Study leader:

Zhang Jinsong 

申请注册联系人电话:

Applicant telephone:

+86 18642047842

研究负责人电话:

Study leader's
telephone:

+86 13066667486

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:

tkl901211@163.com

研究负责人电子邮件:

Study leader's E-mail:

cmu4h-zjs@126.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

Shenyang Aier Excellence Eye Hospital

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:

中国辽宁省沈阳市和平区南宁北街34号

研究负责人通讯地址:

中国辽宁省沈阳市和平区南宁北街34号

Applicant address:

34 Nanning Street North, Heping District, Shenyang, Liaoning, China

Study leader's address:

34 Nanning Street North, Heping District, Shenyang, Liaoning, China

申请注册联系人邮政编码:

Applicant postcode:

110001

研究负责人邮政编码:

Study leader's postcode:

110001

申请人所在单位:

沈阳爱尔卓越眼科医院

Applicant's institution:

Shenyang Aier Excellence Eye Hospital

研究负责人所在单位:

沈阳爱尔卓越眼科医院

Affiliation of the Leader:

Shenyang Aier Excellence Eye Hospital

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:

2023KJB0001

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:

爱尔眼科医院集团伦理委员会

Name of the ethic committee:

Ethics Committee of Aier Eye Hospital Group

伦理委员会批准日期:

Date of approved by ethic committee:

2023-04-18 00:00:00

伦理委员会联系人:

武彬

Contact Name of the ethic committee:

Wu Bin

伦理委员会联系地址:

34 North Street, Nanning

Contact Address of the ethic committee:

34 Nanning Street North, Heping District, Shenyang, Liaoning, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 13940069562

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:

沈阳爱尔卓越眼科医院

Primary sponsor:

Shenyang Aier Excellence Eye Hospital

研究实施负责(组长)单位地址:

中国辽宁省沈阳市和平区南宁北街34号

Primary sponsor's address:

34 Nanning Street North, Heping District, Shenyang, Liaoning, 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):

辽宁

市(区县):

沈阳

Country:

China

Province:

Liaoning

City:

Shenyang

单位(医院):

沈阳爱尔卓越眼科医院

具体地址:

和平区南宁北街34号

Institution
hospital:

Shenyang Aier Excellence Eye Hospital

Address:

34 Nanning Street North, Heping District

经费或物资来源:

高视公司

Source(s) of funding:

GAUSH Corporation

研究疾病:

白内障  

Target disease:

cataract

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:

队列研究 

Study design:

Cohort study 

研究目的:

本研究旨在通过比较白内障患者植入LS-313MF15 区域折射景深延长型人工晶状体与L-313单焦点人工晶状体术后视功能和视觉质量差异来评估LS-313MF15 IOL植入术后患者视程延伸的视功能的优势情况。 同时对合并规则角膜散光的年龄相关性白内障患者植入LS-313MF15T人工晶状体后视觉效果来评估LS-313MF15T IOL植入术后晶状体稳定性及患者视觉质量改善情况。  

Objectives of Study:

The purpose of this study was to evaluate the extension of visual range in cataract patients after implantation of LS-313MF15 IOL by comparing the difference in visual function and visual quality between LS-313MF15 regional refractive depth-of-field extended intraocular lens and L-313 monofocal intraocular lens. The advantage of the visual function. At the same time, the visual effect of age-related cataract patients with regular corneal astigmatism after implantation of LS-313MF15T IOL was evaluated to evaluate the stability of the lens and the improvement of visual quality of patients after LS-313MF15T IOL implantation.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

年龄不小于18岁;具有清晰的认知能力;22mm≤术前轴长≤26.5mm。对照组:角膜散光≤1.0D,单眼植入L-313 IOL;观察组一:角膜散光≤1.0D,单眼植入LS-313MF15 IOL的白内障患者;观察组二:规则角膜散光1.0D~4.0D,单眼植入LS-313MF15T IOL的白内障患者(单眼手术患者选取手术眼入组。双眼手术者以优先手术眼入组)。根据Emery-Little分级系统,双眼核硬度为Ⅰ-Ⅳ级;手术过程顺利没有后囊破裂等并发症(需要在患者术中进行判断)。患者同意签署《受试者知情同意书》。

Inclusion criteria

Aged not less than 18 years old; with clear cognitive ability; 22mm ≤ preoperative axial length ≤ 26.5mm. Control group: corneal astigmatism ≤ 1.0D, with L-313 IOL implanted in one eye; observation group 1: cataract patients with corneal astigmatism ≤ 1.0D, with LS-313MF15 IOL implanted in one eye; observation group 2: regular corneal astigmatism 1.0D~4.0D , cataract patients implanted with LS-313MF15T IOL in one eye (patients with unilateral surgery selected the operated eye, and patients with binocular surgery were selected as the priority operated eye). According to the Emery-Little grading system, the nuclear hardness of both eyes was grade I-IV; the operation went smoothly without complications such as posterior capsule rupture (judgment needs to be made during the operation). The patient agreed to sign the "Subject Informed Consent Form".

排除标准:

高度近视(球镜> -6.0D),术前轴长>26.5mm,角膜不规则散光>1.0D,角膜营养不良,圆锥角膜和其他角膜疾病的患者;瞳孔异常,青光眼,晶状体不全脱位,眼内炎病史,黄斑变性或视网膜病变,神经性眼科疾病或不能耐受手术的患者;因眼部病变预计术后视力可能低于0.63;所需人工晶状体度数在可用范围之外;使用可能影响视力的眼部或全身性药物;有角膜屈光手术病史,内眼手术史或眼外伤史的患者。

Exclusion criteria:

Patients with high myopia (spherical lens > -6.0D), preoperative axial length > 26.5mm, corneal irregular astigmatism > 1.0D, corneal dystrophy, keratoconus and other corneal diseases; pupil abnormalities, glaucoma, lens insufficiency, eye Patients with a history of internal inflammation, macular degeneration or retinopathy, neurological ophthalmic diseases or patients who cannot tolerate surgery; the postoperative visual acuity may be lower than 0.63 due to ocular lesions; the required intraocular lens power is outside the available range; the use may affect vision ocular or systemic medications; patients with a history of corneal refractive surgery, intraocular surgery, or ocular trauma.

研究实施时间:

Study execute time:

From 2023-04-24 00:00:00 To 2024-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-04-24 00:00:00 To 2024-12-31 00:00:00

干预措施:

Interventions:

组别:

观察组一(年龄相关性白内障患者接受白内障超声乳化联合LS-313MF15 IOL植入术)

样本量:

50

Group:

group 1 (Patients with age-related cataract received phacoemulsification combined with LS-313MF15 IOL implantation)

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

观察组二(合并规则角膜散光(角膜散光1.0~4.0D)的年龄相关性白内障患者接受白内障超声乳化联合LS-313MF15T IOL植入术)

样本量:

50

Group:

group 2 (Age-related cataract patients with regular corneal astigmatism (corneal astigmatism 1.0-4.0D) received phacoemulsification combined with LS-313MF15T IOL implantation)

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

组别:

对照组(年龄相关性白内障患者接受白内障超声乳化联合L-313 IOL植入术)

样本量:

50

Group:

control group (Patients with age-related cataract received phacoemulsification combined with L-313 IOL implantation)

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):

辽宁 

市(区县):

沈阳 

Country:

China

Province:

Liaoning

City:

Shenyang

单位(医院):

沈阳爱尔卓越眼科医院 

单位级别:

二级 

Institution
hospital:

Shenyang Aier Excellence Eye Hospital

Level of the institution:

Secondary

国家:

中国

省(直辖市):

辽宁 

市(区县):

沈阳 

Country:

China

Province:

Liaoning

City:

Shenyang

单位(医院):

辽宁爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Liaoning Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

湖南 

市(区县):

长沙 

Country:

China

Province:

Hunan

City:

Changsha

单位(医院):

长沙爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Changsha Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

湖北 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Hunan

单位(医院):

武汉爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Whan

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

重庆 

市(区县):

北京 

Country:

China

Province:

Chongqing

City:

Beijing

单位(医院):

重庆眼科医院 

单位级别:

三级 

Institution
hospital:

Chongqing Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

北京爱尔英智眼科医院 

单位级别:

三级 

Institution
hospital:

Beijing Aier Yingzhi Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

天津 

市(区县):

 

Country:

China

Province:

Tianjin

City:

单位(医院):

天津爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Tianjin Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

安徽 

市(区县):

 

Country:

China

Province:

Anhui

City:

单位(医院):

合肥爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Hefei Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

广西壮族自治区 

市(区县):

 

Country:

China

Province:

Guangxi Zhuang Autonomous Region

City:

单位(医院):

南宁爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Nanning Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

深圳爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Shenzhen Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

陕西 

市(区县):

 

Country:

China

Province:

Shanxi

City:

单位(医院):

西安爱尔古城眼科医院 

单位级别:

三级 

Institution
hospital:

Xi'an Aier Ancient City Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

新疆 

市(区县):

 

Country:

China

Province:

Xinjiang

City:

单位(医院):

乌鲁木齐爱尔眼科医院 

单位级别:

三级 

Institution
hospital:

Urumqi Aier Eye Hospital

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

山西 

市(区县):

 

Country:

China

Province:

Shanxi

City:

单位(医院):

山西太原爱尔 

单位级别:

三级 

Institution
hospital:

Shanxi Taiyuan Aier

Level of the institution:

Tertiary

国家:

中国

省(直辖市):

山东 

市(区县):

 

Country:

China

Province:

Shandong

City:

单位(医院):

山东烟台爱尔 

单位级别:

三级 

Institution
hospital:

Shandong Yantai Aier

Level of the institution:

Tertiary

测量指标:

Outcomes:

指标中文名:

5m最佳矫正视力

指标类型:

主要指标

Outcome:

5m BCVA

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

离焦曲线

指标类型:

主要指标

Outcome:

Defocus curve

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

验光及眼压

指标类型:

次要指标

Outcome:

optometry and IOP

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后观察组二LS-313MF15T IOL人工晶状体旋转度(术后1月、3月)

指标类型:

次要指标

Outcome:

Postoperative observation group II LS-313MF15T IOL intraocular lens rotation (1m and 3m after operation)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

40cm、60cm、5m裸眼视力及5m远视力矫正下中距离视力(60cm)和5m远视力矫正下近距离视力(40cm)(术后1月、3月)

指标类型:

次要指标

Outcome:

40cm, 60cm, 5m UCVA and 5m DCVA with intermediate distance vision (60cm) and 5m distance vision correction with near distance vision (40cm) (1m, 3m after operation)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

眼内像差、MTF值

指标类型:

次要指标

Outcome:

Wavefront aberration and MTF curve

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:

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 80 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):

术前常规交代,根据患者自愿选择自动分组

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

Routine explanation before surgery, automatic grouping according to the patient's voluntary choice

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:

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):

临床试验公共管理平台 网址http://www.medresman.org.cn/login.aspx

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

Clinical Trial Management Public Platform http://www.medresman.org.cn/login.aspx

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:

Electronic Data Capture, EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2023-04-23 17:59:20