ChiCTR2400082285 版本V1.0 版本创建时间2024/03/26 10:20:07 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:

ChiCTR2400082285 

最近更新日期:

Date of Last Refreshed on:

2024-03-26 10:19:42 

注册时间:

Date of Registration:

2024-03-26 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

臂式电子血压计整体有效性评估临床试验

Public title:

Clinical Trial to Evaluate the Overall Effectiveness of an Arm-Mounted Electronic Sphygmomanometer

注册题目简写:

English Acronym:

研究课题的正式科学名称:

臂式电子血压计整体有效性评估临床试验

Scientific title:

Clinical Trial to Evaluate the Overall Effectiveness of an Arm-Mounted Electronic Sphygmomanometer

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:

韩政通 

研究负责人:

王桂琦 

Applicant:

Zhengtong Han 

Study leader:

Guiqi Wang 

申请注册联系人电话:

Applicant telephone:

+86 155 3217 7433

研究负责人电话:

Study leader's
telephone:

+86 186 3388 9761

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:

zhengtong.han@care-real.com

研究负责人电子邮件:

Study leader's E-mail:

wangguiqi2011@126.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:

浙江省杭州市临平区杭州余杭经济技术开发区五洲路365 号

研究负责人通讯地址:

石家庄市裕华区东岗路89号

Applicant address:

No. 365 Wuzhou Road, Hangzhou Yuhang Economic and Technological Development Zone, Linping District, Hangzhou City, Zhejiang Province, P.R. China

Study leader's address:

89 Donggang Road, Yuhua District, Shijiazhuang, 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:

浙江健拓医疗仪器科技有限公司

Applicant's institution:

JOYTECH Healthcare Co.,Ltd.

研究负责人所在单位:

河北医科大学第一医院

Affiliation of the Leader:

The First Hospital of Hebei Medical University

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:

[2024]临审第(685)号

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:

河北医科大学第一医院药物临床试验伦理委员会

Name of the ethic committee:

Ethics Committee for Drug Clinical Trials of the First Hospital of Hebei Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2024-01-17 00:00:00

伦理委员会联系人:

杨谦谦

Contact Name of the ethic committee:

Qianqian Yang

伦理委员会联系地址:

石家庄市裕华区东岗路89号

Contact Address of the ethic committee:

89 Donggang Road, Yuhua District, Shijiazhuang, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 156 3040 0256

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:

河北医科大学第一医院

Primary sponsor:

The First Hospital of Hebei Medical University

研究实施负责(组长)单位地址:

石家庄市裕华区东岗路89号

Primary sponsor's address:

89 Donggang Road, Yuhua District, Shijiazhuang, 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):

浙江省

市(区县):

杭州市

Country:

China

Province:

Zhejiang

City:

Hangzhou

单位(医院):

浙江健拓医疗仪器科技有限公司

具体地址:

浙江省杭州市临平区杭州余杭经济技术开发区五洲路365 号

Institution
hospital:

JOYTECH Healthcare Co.,Ltd.

Address:

No. 365 Wuzhou Road, Hangzhou Yuhang Economic and Technological Development Zone, Linping District, Hangzhou City, Zhejiang Province, P.R. China

经费或物资来源:

浙江健拓医疗仪器科技有限公司

Source(s) of funding:

JOYTECH Healthcare Co.,Ltd.

研究疾病:

血压  

Target disease:

blood pressure

研究疾病代码:

Target disease code:

研究类型:

诊断试验

Study type:

Diagnostic test

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

诊断试验诊断准确性 

Study design:

Diagnostic test for accuracy 

研究目的:

评估臂式电子血压计的整体有效性和安全性  

Objectives of Study:

Assessing the overall effectiveness and safety of arm-mounted electronic sphygmomanometers

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)年龄>12 周岁,性别不限; 2)自愿参加血压测量并签署知情同意书; 3)能够与研究医生良好沟通,依从性较好,可遵循临床研究的要求。

Inclusion criteria

(1) Age > 12 years old, gender is not limited; 2) Voluntarily participate in blood pressure measurement and sign an informed consent form; 3) Able to communicate well with the study physicians and have good compliance to follow the requirements of the clinical study.

排除标准:

1)对血压袖带材料过敏; 2)严重心律不齐者; 3)意识障碍者,不能充分给予知情; 4)研究者认为其他不宜参加本研究。

Exclusion criteria:

1) Hypersensitivity to blood pressure cuff materials; 2) Persons with severe cardiac arrhythmias; 3) Persons with impaired consciousness who are unable to give adequate information; 4) Others who, in the opinion of the investigator, should not participate in this study.

研究实施时间:

Study execute time:

From 2024-03-11 00:00:00 To 2024-11-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-04-08 00:00:00 To 2024-11-30 00:00:00

诊断试验:

Diagnostic Tests:

金标准或参考标准(即可准确诊断某疾病的单项方法或多项联合方法,在本研究中用于诊断是否有该病的临床参考标准):

水银血压计血压测量

Gold Standard or Reference Standard (The clinical reference standards required to establish the presence or absence of the target condition in the tested population in present study):

Mercury Sphygmomanometer Blood Pressure Measurement

指标试验(即本研究的待评估诊断试验,无论为方法、生物标志物或设备,均请列出名称):

臂式电子血压计血压测量

Index test:

Blood Pressure Measurement with Arm-mounted Electronic Sphygmomanometer

目标人群(可以是某种疾病患者或正常人群,详细描述其疾病特征,注意应纳入符合分布特点的全序列病例,具有良好的代表性)

正常人群

例数:

Sample size:

85

Target condition (The target condition is a particular disease or disease stage that the index test will be intended to identify. Please specify the characteristics in detail; the population should has a complete spectrum and good representative):

the normal population

容易混淆的疾病人群(即与目标疾病不易区分的一种或多种不同疾病,应避免采用正常人群对照的病例-对照设计):

例数:

Sample size:

0

Population with condition difficult to distinguish from the target condition, the normal population in a case-control study design should be avoid:

NA

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

河北省 

市(区县):

石家庄市 

Country:

China

Province:

Hebei Province

City:

Shijiazhuang

单位(医院):

河北医科大学第一医院 

单位级别:

三甲 

Institution
hospital:

The First Hospital of Hebei Medical University

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

内蒙古自治区 

市(区县):

呼和浩特 

Country:

China

Province:

Inner Mongolia Autonomous Region

City:

Hohhot

单位(医院):

内蒙古自治区人民医院 

单位级别:

三甲 

Institution
hospital:

Inner Mongolia Autonomous Region People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

血压测量准确性

指标类型:

主要指标

Outcome:

Blood pressure measurement accuracy

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

脉率测量准确性

指标类型:

次要指标

Outcome:

Accuracy of pulse rate measurement

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

器械性能评价

指标类型:

次要指标

Outcome:

Evaluation of instrument performance

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

器械缺陷

指标类型:

次要指标

Outcome:

Instrument defects

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:

NA

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

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 12 years
最大 Max age NA 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):

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

NA

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

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):

发表文献

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

Published Literature

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:

病历报告表

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

Case Report Form

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:

 2024-03-26 10:19:42