根據醫療器材促進協會/歐洲高血壓學會/國際標準化組織通用標準,對AOJ-33A示波法血壓計在一般人群中的適用性進行驗證

注册号:

Registration number:

ChiCTR2600124597 

最近更新日期:

Date of Last Refreshed on:

2026-05-14 11:17:57 

注册时间:

Date of Registration:

2026-05-14 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

根據醫療器材促進協會/歐洲高血壓學會/國際標準化組織通用標準,對AOJ-33A示波法血壓計在一般人群中的適用性進行驗證

Public title:

Validation of the AOJ-33A oscillometric blood pressure monitor in the general population according to the association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Universal Standard

注册题目简写:

English Acronym:

研究课题的正式科学名称:

根據醫療器材促進協會/歐洲高血壓學會/國際標準化組織通用標準,對AOJ-33A示波法血壓計在一般人群中的適用性進行驗證

Scientific title:

Validation of the AOJ-33A oscillometric blood pressure monitor in the general population according to the association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Universal Standard

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:

林子山 

研究负责人:

林子山 

Applicant:

LAM Chi Shan 

Study leader:

LAM Chi Shan 

申请注册联系人电话:

Applicant telephone:

+852 5928 6927

研究负责人电话:

Study leader's
telephone:

+852 5928 6927

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:

chishan.lam@link.cuhk.edu.hk

研究负责人电子邮件:

Study leader's E-mail:

ahnndhana_team@ha.org.hk

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:

香港新界大埔全安路 11 號雅麗氏何妙齡那打素醫院C3 麻醉及手術服務部

研究负责人通讯地址:

香港新界大埔全安路 11 號雅麗氏何妙齡那打素醫院C3 麻醉及手術服務部

Applicant address:

Department of Anaesthesiology and Operating Services, 3rd Floor, Block C, Alice Ho Miu Ling Nethersole Hospital, 11 Chuen On Road, Tai Po, N.T., Hong Kong SAR

Study leader's address:

Department of Anaesthesiology and Operating Services, 3rd Floor, Block C, Alice Ho Miu Ling Nethersole Hospital, 11 Chuen On Road, Tai Po, N.T., Hong Kong SAR

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:

醫院管理局雅麗氏何妙齡那打素醫院及北區醫院 麻醉及手術服務部

Applicant's institution:

Department of Anaesthesiology and Operating Services, Alice Ho Miu Ling Nethersole Hospital and North District Hospital, Hospital Authority

研究负责人所在单位:

醫院管理局雅麗氏何妙齡那打素醫院及北區醫院 麻醉及手術服務部

Affiliation of the Leader:

Department of Anaesthesiology and Operating Services, Alice Ho Miu Ling Nethersole Hospital and North District Hospital, Hospital Authority

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:

2026.262

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:

香港中文大學 – 新界東醫院聯網臨床研究倫理聯席委員會

Name of the ethic committee:

The Joint CUHK-NTEC CREC

伦理委员会批准日期:

Date of approved by ethic committee:

2026-05-03 00:00:00

伦理委员会联系人:

Envy LEE

Contact Name of the ethic committee:

Envy LEE

伦理委员会联系地址:

香港沙田威爾斯親王醫院呂志和臨床醫學大樓8樓

Contact Address of the ethic committee:

8/F, Lui Che Woo Clinical Sciences Building, Prince of Wales Hospital Shatin, Hong Kong SAR

伦理委员会联系人电话:

Contact phone of the ethic committee:

+852 3505 3935

伦理委员会联系人邮箱:

Contact email of the ethic committee:

crec@cuhk.edu.hk

研究实施负责(组长)单位:

醫院管理局雅麗氏何妙齡那打素醫院及北區醫院 麻醉及手術服務部

Primary sponsor:

Department of Anaesthesiology and Operating Services, Alice Ho Miu Ling Nethersole Hospital and North District Hospital, Hospital Authority

研究实施负责(组长)单位地址:

香港新界大埔全安路 11 號雅麗氏何妙齡那打素醫院C3 麻醉及手術服務部

Primary sponsor's address:

Department of Anaesthesiology and Operating Services, 3rd Floor, Block C, Alice Ho Miu Ling Nethersole Hospital, 11 Chuen On Road, Tai Po, N.T., Hong Kong SAR

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中國

省(直辖市):

香港特別行政區

市(区县):

Country:

China

Province:

Hong Kong SAR

City:

单位(医院):

醫院管理局雅麗氏何妙齡那打素醫院及北區醫院 麻醉及手術服務部

具体地址:

香港新界大埔全安路 11 號雅麗氏何妙齡那打素醫院C3 麻醉及手術服務部

Institution
hospital:

Department of Anaesthesiology and Operating Services, Alice Ho Miu Ling Nethersole Hospital and North District Hospital, Hospital Authority

Address:

Department of Anaesthesiology and Operating Services, 3rd Floor, Block C, Alice Ho Miu Ling Nethersole Hospital, 11 Chuen On Road, Tai Po, N.T., Hong Kong SAR

经费或物资来源:

醫院管理局雅麗氏何妙齡那打素醫院及北區醫院 麻醉及手術服務部

Source(s) of funding:

Department of Anaesthesiology and Operating Services, Alice Ho Miu Ling Nethersole Hospital and North District Hospital, Hospital Authority

研究疾病:

无  

Target disease:

None

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:

横断面 

Study design:

Cross-sectional 

研究目的:

根據 ISO 81060-2:2018 標準,評估自動血壓計測量收縮壓和舒張壓的準確性,並與使用水銀血壓計進行手動聽診進行比較。  

Objectives of Study:

To assess the accuracy of the automated BP device in measuring systolic and diastolic blood pressure against manual auscultation using a mercury sphygmomanometer, in accordance with ISO 81060-2:2018.

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:

1. 懷孕 2. 嚴重週邊血管疾病 3. 無法保持坐姿5分鐘 4. 嚴重心律不整 5. 任何妨礙使用左手臂測量血壓的情況(例如局部皮膚傷口/感染、骨折、先前影響淋巴系統的左側乳房手術)

Exclusion criteria:

1.Pregnancy 2.Severe peripheral vascular disease 3.Inability to remain seated for 5 minutes 4.Severe arrhythmia 5.Any condition that prohibits the use of left arm for blood pressure measurement (e.g. local skin wound/infection, bone fracture, previous left breast operation affecting the lymphatic system)

研究实施时间:

Study execute time:

From 2026-06-01 00:00:00 To 2026-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2026-06-01 00:00:00 To 2026-12-31 00:00:00

干预措施:

Interventions:

组别:

观察组

样本量:

105

Group:

Observation group

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:

中國

省(直辖市):

香港特別行政區 

市(区县):

 

Country:

China

Province:

Hong Kong SAR

City:

单位(医院):

雅麗氏何妙齡那打素醫院 

单位级别:

无 

Institution
hospital:

Alice Ho Miu Ling Nethersole Hospital

Level of the institution:

N/A

测量指标:

Outcomes:

指标中文名:

計算收縮壓和舒張壓的設備讀數與參考讀數之間的平均差異(MD)和標準差(SD)

指标类型:

主要指标

Outcome:

Calculate mean difference (MD) and standard deviation (SD) between device and reference readings for systolic and diastolic BP.

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:

组织:

Sample Name:

None

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 18 years
最大 Max age 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):

None

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:

None

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):

ResMan 临床试验公共管理平台Clinical Trial Management Public Platform (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 Clinical Trial Management Public Platform (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:

标准化的数据收集和管理系统包括纸质的病例记录表(Case Record Form)、ResMan (www.medresman.org) 电子数据采集和管理系统(Electronic Data Capture, EDC)

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

A standard data collection and management system include a CRF and an electronic data capture such as ResMan (www.medresman.org)

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:

 2026-05-14 11:17:33