0.1%他克莫司(FK506)治疗干燥综合征眼部临床疗效评价

注册号:

Registration number:

ChiCTR-OIB-16007789 

最近更新日期:

Date of Last Refreshed on:

2016-01-18 20:09:37 

注册时间:

Date of Registration:

2015-12-30 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

0.1%他克莫司(FK506)治疗干燥综合征眼部临床疗效评价

Public title:

0.1%Tacrolimus (FK506) in the treatment of sjogren's syndrome clinical efficacy evaluation

注册题目简写:

English Acronym:

研究课题的正式科学名称:

0.1%他克莫司(FK506)治疗干燥综合征眼部临床疗效评价

Scientific title:

0.1%Tacrolimus (FK506) in the treatment of sjogren's syndrome clinical efficacy evaluation

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:

杨舒 

研究负责人:

刘祖国 

Applicant:

Shu Yang 

Study leader:

Zuguo Liu 

申请注册联系人电话:

Applicant telephone:

+86 13606935286

研究负责人电话:

Study leader's
telephone:

+86 18959289999

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:

yangshujjx@163.com

研究负责人电子邮件:

Study leader's E-mail:

zuguoliu@xmu.edu.cn

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:

福建省厦门市厦门大学翔安校区医学院成义楼402

研究负责人通讯地址:

福建省厦门市厦门大学翔安校区医学院成义楼402

Applicant address:

4th Floor, Chengyi Bulding, Xiang-an campus of Xiamen University, South Xiang-an Road, Xiamen, Fujian, China

Study leader's address:

4th Floor, Chengyi Bulding, Xiang-an campus of Xiamen University, South Xiang-an Road, Xiamen, Fujian, 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:

厦门大学眼科研究所

Applicant's institution:

Eye Institute of Xiamen University

研究负责人所在单位:

Affiliation of the Leader:

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:

2015006

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:

厦门大学眼科研究所医学伦理委员会

Name of the ethic committee:

Xiamen university institute of ophthalmology medical ethics committee

伦理委员会批准日期:

Date of approved by ethic committee:

2015-12-16 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:

厦门大学眼科研究所

Primary sponsor:

Eye Institute of Xiamen University

研究实施负责(组长)单位地址:

福建省厦门市厦门大学翔安校区医学院成义楼402

Primary sponsor's address:

4th Floor, Chengyi Bulding, Xiang-an campus of Xiamen University, South Xiang-an Road, Xiamen, Fujian, 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):

福建省

市(区县):

厦门市

Country:

China

Province:

Fujian

City:

Xiamen

单位(医院):

厦门大学眼科研究所

具体地址:

福建省厦门市翔安南路厦门大学翔安校区医学院成义楼402

Institution
hospital:

Eye Institute of Xiamen University

Address:

4th Floor, Chengyi Bulding, Xiang-an campus of Xiamen University, South Xiang-an Road, Xiamen, Fujian, China

经费或物资来源:

日本千寿制药株式会社

Source(s) of funding:

Senju Pharmaceutical Co., Ltd.

研究疾病:

干燥综合征  

Target disease:

Sjogren's syndrome

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:

IV期临床试验 

Study phase:

4

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

通过临床实验评价0.1%他克莫司(FK506)治疗干燥综合征眼征疗效  

Objectives of Study:

Through the clinical experiment evaluation 0.1% tacrolimus (FK506) eye dryness syndrome curative effect

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:

排除标准:
凡有下列情况之一者,不作为入选病例:
(1) 对试验药物中任何成分过敏者。
(2) 孕妇或哺乳期女性或近期有生育计划者。
(3) 临床上拟诊为真菌、细菌角、结膜炎活动期患者。
(4) 合并有其他结膜、角膜和虹膜明显病变者。
(5) 合并有严重心、脑血管、肝、肾及造血系统等严重原发病。
(6) 近六个月内有内眼手术或眼部外伤者。
(7) 绝经妇女激素替代治疗。
(8) 近1月内接受泪小点栓塞治疗。
(9) 青光眼或出现过眼压高的患者。
(10) 可能影响结果的治疗(如全身类同醇激素、免疫抑制治疗)。
(11) 试验期间无法停戴角膜接触镜者。
(12) 全身或眼部长期用药可能影响研究评估患者。
(14)在试验期间无法保证按要求用药及随访者。

Exclusion criteria:

Exclusion criteria: Every one of the following circumstances, not as the case:
(1) the test allergy to any ingredient in the drug;
(2) pregnant or lactating women or recently have fertility planners;
(3) the clinical examination for fungi, bacteria, Angle, conjunctivitis in active patients;
(4) with other conjunctiva, cornea and iris obvious pathological changes;
(5) with serious heart, cerebrovascular, liver, kidney and hematopoietic system, severe primary disease;
(6) nearly six months have eye surgery within or outside of the injured eye;
(7) postmenopausal hormone replacement therapy;
(8) lacrimal point embolism therapy nearly 1 month;
(9) high intraocular pressure of patients with glaucoma or seen;
(10) may affect the outcome of treatment, such as systemic steroid hormones and immunosuppressive therapy);
(11) experiments cannot stop wearing corneal contact lens;
(12) patients with systemic or ocular long-term drug use may affect the research assessment;
(13) during the test is no guarantee that drugs according to the requirements and with the visitor.

研究实施时间:

Study execute time:

From 2016-01-18 00:00:00 To 2016-05-18 00:00:00  

征募观察对象时间:

Recruiting time:

From 2016-01-18 00:00:00 To 2016-05-18 00:00:00

干预措施:

Interventions:

组别:

他克莫司组治疗组

样本量:

30

Group:

Tacrolimus therapy group

Sample size:

干预措施:

0.1%FK506+0.1%玻璃酸钠滴眼 一天两次 30天

干预措施代码:

Intervention:

0.1% FK506 + 0.1% sodium hyaluronate eye drops Twice a day for 30 days

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

福建 

市(区县):

厦门 

Country:

China

Province:

Fujian

City:

Xiamen

单位(医院):

厦门大学附属厦门眼科中心 

单位级别:

三级甲等 

Institution
hospital:

Xiamen University affiliated Xiamen Eye Center

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

干眼问卷

指标类型:

主要指标

Outcome:

dry eye questionnaire

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

视力

指标类型:

主要指标

Outcome:

vision

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

结膜水肿

指标类型:

主要指标

Outcome:

conjunctival chemosis

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

结膜充血

指标类型:

主要指标

Outcome:

conjunctival congestion

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

睑缘改变

指标类型:

主要指标

Outcome:

eyelid edge change

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

睑板腺分泌能力

指标类型:

主要指标

Outcome:

Meibomian gland secretion capacity

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

睑板腺分泌物性质

指标类型:

主要指标

Outcome:

The nature of the meibomian gland secretion

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

角膜混浊

指标类型:

主要指标

Outcome:

corneal opacity

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

角膜新生血管

指标类型:

主要指标

Outcome:

corneal neovascularization

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

角膜水肿

指标类型:

主要指标

Outcome:

corneal edema

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

泪河高度

指标类型:

主要指标

Outcome:

tear meniscus height

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

泪膜破裂时间

指标类型:

主要指标

Outcome:

TBUT

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

泪液分泌实验

指标类型:

主要指标

Outcome:

schirmer I test

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

角膜共聚焦显微镜

指标类型:

主要指标

Outcome:

confocal microscope

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:

标本中文名:

印迹细胞

组织:

结膜组织

Sample Name:

impression cytology

Tissue:

conjuncitva tissue

人体标本去向

使用后销毁  

说明

使用后销毁

Fate of sample:

Destruction after use  

Note:

Use after destruction

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 70 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):

符合入选标准的患者直接用药,定时复查

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

Meet the criteria for the patients with medication directly, regular review

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

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):

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

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:

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

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2016-01-18 20:09:37