ChiCTR2100051713 版本V1.4 版本创建时间2021/10/03 11:49:55 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:

ChiCTR2100051713 

最近更新日期:

Date of Last Refreshed on:

2021-10-03 11:49:29 

注册时间:

Date of Registration:

2021-10-01 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

中国人眼颅压力梯度的临床研究

Public title:

Clinical study on the reference interval of Chinese Intraocular and Intracranial Pressure Gradient (ONPG)

注册题目简写:

English Acronym:

研究课题的正式科学名称:

中国人眼颅压力梯度参考区间的临床研究

Scientific title:

Clinical study on the reference interval of Chinese Intraocular and Intracranial Pressure Gradient (ONPG)

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:

林丹婷 

研究负责人:

王宁利 

Applicant:

Danting Lin 

Study leader:

Ningli Wang 

申请注册联系人电话:

Applicant telephone:

+86 18810671803

研究负责人电话:

Study leader's telephone:

+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:

ldtldld@163.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:

北京市东城区崇文门内大街8号

研究负责人通讯地址:

北京市东城区崇文门内大街8号

Applicant address:

8 Chong-Wen-Men-Nei Street, Dongcheng District, Beijing, China

Study leader's address:

8 Chong-Wen-Men-Nei Street, Dongcheng District, Beijing, 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:

首都医科大学附属北京同仁医院

Applicant's institution:

Beijing Tongren Hospital

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

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:

TRECKY2021-62

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:

首都医科大学附属北京同仁医院伦理委员会

Name of the ethic committee:

The Medical Ethics Committee of Beijing Tongren Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2021-04-01 00:00:00

伦理委员会联系人:

常灏

Contact Name of the ethic committee:

Hao Chang

伦理委员会联系地址:

北京市东城区崇文门内大街8号

Contact Address of the ethic committee:

8 Chong-Wen-Men-Nei Street, 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

研究实施负责(组长)单位地址:

北京市东城区崇文门内大街8号

Primary sponsor's address:

8 Chong-Wen-Men-Nei Street, Dongcheng District, Beijing, 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):

北京

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

首都医科大学附属北京同仁医院

具体地址:

东城区崇文门内大街8号

Institution
hospital:

Beijing Tongren Hospital

Address:

8 Chong-Wen-Men-Nei Street, Dongcheng District

经费或物资来源:

国家自然科学基金

Source(s) of funding:

National Natural Science Foundation

Target disease:

glaucoma

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

探讨中国人群眼颅压力梯度参考区间,为建立基于眼颅压力梯度的开角型青光眼诊疗新体系提供理论标准。  

Objectives of Study:

To establish the normal reference interval of the intracranial pressure gradient in the Chinese population so as to provide a standard for the establishment of open-angle glaucoma diagnosis and treatment new system based on the Intraocular and Intracranial Pressure Gradient (ONPG).

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)神经内科需行腰椎穿刺且同意配合进行病史采集、眼压及其他全身参数测量的患者;
(2)经病史采集,患者年龄、性别、体重、身高、体质指数(Body mass index,BMI) 及平均动脉血压(Mean artery blood pressure,MABP)等基本信息齐全者;

Inclusion criteria

1.Patients in the neurology department who requiring lumbar puncture and voluntary to participate the research;
2.Patients with complete basic information such as age, gender, weight, height, body mass index (BMI) and mean artery blood pressure (MABP).

排除标准:

(1)存在脑水肿、颅脑炎性疾病、CT显示有颅内占位病变、出血、肿瘤等全身性疾病患者;
(2)高血压、糖尿病且出现高血压脑病、糖尿病酸中毒者;
(3)具有服用维生素 A 类药物或四环素类药物等继发性颅压改变者;
(4)青光眼、甲状腺眼病等其他造成眼压改变病变者。

Exclusion criteria:

1.Patients with diseases such as brain edema, encephalitis, CT findings of intracranial space-occupying lesions,hemorrhage, tumors, abnormal intracranial pressure, etc.;
2.Hypertensive encephalopathy and diabetic acidosis due to hypertension and diabetes;
3.Patients with secondary intracranial pressure changes such as taking vitamin A or tetracycline drugs;
4.Glaucoma,thyroid ophthalmopathy and other diseases which cause changes in intraocular pressure.

研究实施时间:

Study execute time:

From 2019-09-01 00:00:00 To 2023-10-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2019-09-01 00:00:00 To 2023-10-01 00:00:00  

干预措施:

Interventions:

组别:

Case series

样本量:

1000

Group:

Case series

Sample size:

干预措施:

干预措施代码:

Intervention:

Nil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China 

Province:

Beijing 

City:

 

单位(医院):

首都医科大学附属北京同仁医院 

单位级别:

三甲 

Institution
hospital:

Beijing Tongren Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

颅压

指标类型:

主要指标

Outcome:

intracranial pressure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

眼压

指标类型:

主要指标

Outcome:

intraocular pressure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

眼光学相干断层成像

指标类型:

次要指标

Outcome:

optical coherence tomography

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

眼底相干光层析血管成像

指标类型:

次要指标

Outcome:

optical coherence tomography angiography

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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 90 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):

不适用

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

N/A

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:

N/A

Blinding:

N/A

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):

ResMan, http://www.medresman.org.cn.

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

ResMan, http://www.medresman.org.cn.

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:

CRF表采集

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

CRF collection

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2021-10-01 19:05:58