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CompletedNCT04931264

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

Validation of the YuWell YE660D Oscillometric Upper-arm Blood Pressure Monitor for Clinic and Home in General Population According to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
92 (actual)
Sponsor
The Second Hospital of Nanjing Medical University · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Accepted

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

Interventions

TypeNameDescription
DIAGNOSTIC_TESTYuWell YE660D Electronic SphygmomanometerMeasurement blood pressure by YuWell YE660D Electronic Sphygmomanometer and Desk Mercury Sphygmomanometer

Timeline

Start date
2021-09-01
Primary completion
2022-03-01
Completion
2022-03-08
First posted
2021-06-18
Last updated
2022-03-10

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04931264. Inclusion in this directory is not an endorsement.

Clinical Trial of YuWell YE660D Blood Pressure Monitor in General Population According to the ISO 81060-2:2018 (NCT04931264) · Clinical Trials Directory