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Clinical Trial of YuWell YE660D Blood Pressure Monitor in General Population According to the ISO 81060-2:2018

NCT04931264 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 92

Last updated 2022-03-10

No results posted yet for this study

Summary

The purpose of this study is to evaluate the accuracy of the YuWell YE660D oscillometric upper-arm blood pressure monitor for clinic and home in general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2:2018).

Conditions

  • Blood Pressure

Interventions

DIAGNOSTIC_TEST

YuWell YE660D Electronic Sphygmomanometer

Measurement blood pressure by YuWell YE660D Electronic Sphygmomanometer and Desk Mercury Sphygmomanometer

Sponsors & Collaborators

  • Jiangsu Yuyue medical equipment & supply Co., Ltd.

    collaborator UNKNOWN

  • The Second Hospital of Nanjing Medical University

    lead OTHER

Principal Investigators

  • Mingzhi Long, MD，PHD · The Second Hospital of Nanjing Medical University

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2022-03-01
Completion
2022-03-08

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04931264 on ClinicalTrials.gov