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Clinical Trial of YuWell YE900 Electronic Sphygmomanometer

NCT04379323 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 92

Last updated 2020-08-19

No results posted yet for this study

Summary

The purpose of this study is to evaluate the accuracy of the YuWell YE900 medical electronic blood pressure monitor for blood pressure measurements in adults and children 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 YE900 Electronic Sphygmomanometer

Measurement blood pressure by YuWell YE900 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
3 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-05-12
Primary Completion
2020-06-17
Completion
2020-07-10

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 NCT04379323 on ClinicalTrials.gov