|
注册号: Registration number: |
ChiCTR-IOR-17013925 |
|
最近更新日期: Date of Last Refreshed on: |
2017-12-14 22:00:58 |
|
注册时间: Date of Registration: |
2017-12-14 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
人工晶状体(非球面)用于白内障摘除手术的安全性和有效性多中心、随机、开放、阳性平行对照临床试验 |
|
Public title: |
Intraocular lens (aspherical) is used for the safety and efficacy of cataract extraction with multiple centers, randomized, open, and positive parallel controlled clinical trials |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
人工晶状体(非球面)用于白内障摘除手术的安全性和有效性多中心、随机、开放、阳性平行对照临床试验 |
|
Scientific title: |
Intraocular lens (aspherical) is used for the safety and efficacy of cataract extraction with multiple centers, randomized, open, and positive parallel controlled clinical trials |
|
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: |
廖向国 |
研究负责人: |
王宁利 |
|
Applicant: |
Xiangguo Liao |
Study leader: |
Ningli Wang |
|
申请注册联系人电话: Applicant telephone: |
+86 18762638310 |
研究负责人电话:
Study leader's |
+86 13511026669 |
|
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: |
lxglmsk@wx-visionpro.com |
研究负责人电子邮件: Study leader's E-mail: |
wningli@vip.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: |
无锡市楝泽路29号科教软件园17号1楼 |
研究负责人通讯地址: |
北京市东城区后沟胡同17号 |
|
Applicant address: |
Floor 1, 17th Building, Software Park, 29 Lianze Road, Wuxi, Jiangsu, China |
Study leader's address: |
17 Hougou alley, Dongcheng District, Beijing, China |
|
申请注册联系人邮政编码: Applicant postcode: |
214125 |
研究负责人邮政编码: Study leader's postcode: |
|
|
申请人所在单位: |
无锡蕾明视康科技有限公司 |
||
|
Applicant's institution: |
Wuxi Vision Pro LTD |
||
|
研究负责人所在单位: |
首都医科大学附属北京同仁医院 |
||
|
Affiliation of the Leader: |
Beijing Tongren Hospital Affiliated to Capital Medical University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
TREC2013-23 |
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: |
首都医科大学附属北京同仁医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethinic committee of Beijing Tongren Hospital Affiliated to Capital Medical University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2013-10-21 00:00:00 | ||
|
伦理委员会联系人: |
韩小茜 |
||
|
Contact Name of the ethic committee: |
Qianxiao Han |
||
|
伦理委员会联系地址: |
北京市东城区后沟胡同17号 |
||
|
Contact Address of the ethic committee: |
17 Hougou alley, Dongcheng District, Beijing, 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: |
首都医科大学附属北京同仁医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Beijing Tongren Hospital Affiliated to Capital Medical University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
17 Hougou alley, Dongcheng District, Beijing, China |
||||||||||||||||||||||
|
Primary sponsor's address: |
17 Hougou alley, Dongcheng District, Beijing, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
无锡蕾明视康科技有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Wuxi Vision Pro LTD |
||||||||||||||||||||||
|
研究疾病: |
白内障 |
||||||||||||||||||||||
|
Target disease: |
Cataract |
||||||||||||||||||||||
|
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: |
验证无锡蕾明视康科技有限公司生产的 RS60A、RS57A、RS55A 型人工晶状体应用于白内障患者治疗的安全性和有效性。 |
||||||||||||||||||||||
|
Objectives of Study: |
To verify the safety and efficacy of RS60A, RS57A and RS55A in the treatment of cataract patients by Wuxi Vision Pro LTD. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
l)合并其他眼部疾病,如先天性小眼球,青光眼,角膜营养不良,黄斑病变/色素上皮细胞病变,糖尿病视网膜病变,严重的视神经萎缩,,慢性葡萄膜炎,严重的前房过浅,脉络膜出血,睫状小带分离(不能固定人工晶状体)等; |
||||||||||||||||||||||
|
Exclusion criteria: |
With other eye diseases, such as congenital microphthalmia, glaucoma, corneal malnutrition, macular degeneration/pigment epithelial lesions, diabetic retinopathy, optic atrophy, and chronic uveitis, serious too shallow anterior chamber, choroid bleeding, ciliary zonule separating fixed intraocular lens (can't), etc.; The eye has retinal detachment or retinopathy; Traumatic cataract or congenital bilateral cataract; Need eye joint operation; The researchers determined that the non-operative eye ignored the function; The corneal endothelial cell count is less than 1000 / mm2; Patients with ocular trauma or intraocular surgery for nearly 3 months; Participated in other drug or medical device clinical trials within 30 days of screening;Patients with severe or unstable heart, liver, kidney, lung, endocrine (including incomplete thyroid function), blood, mental and neurological disorders, etc.; The results of an electrocardiogram or laboratory examination may indicate that there are surgical contraindications; diabetic; ALTAST exceeds the normal value limit of 1.5 times, creatinine exceeds the normal value upper limit; The use of local or systemic drugs may affect the visual acuity during or during the study period; Planned to be pregnant within six months; Unsupervised or unable to follow the doctor's orders; The researchers judged that patients were not eligible for other situations. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2013-04-08 00:00:00至 To 2015-04-18 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2013-04-08 00:00:00 至 To 2015-04-18 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
结束 /Completed |
年龄范围: Participant age: |
|
||||||
|
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): |
Not stated |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
Not stated |
||||||||
|
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 |
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): |
通过ResMan提供原始数据查询 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
IPD will be public accessable via ResMan |
|
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: |
Not stated |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Not stated |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |