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

The Second Hospital of Nanjing Medical University92 enrolled

Overview

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).

Study Type

INTERVENTIONAL

Allocation

Purpose

DIAGNOSTIC

Masking

NONE

Enrollment

Conditions

Blood Pressure

Interventions

YuWell YE660D Electronic SphygmomanometerDIAGNOSTIC_TEST

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

Eligibility

Sex: ALLMin age: 12 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * 12 Years and older; * Subjects voluntarily participate in the clinical trial and sign the informed consent. Exclusion Criteria: * Disturbance of consciousness; * Patients requiring hemodialysis; * Taking anticoagulant drugs due to cardiovascular and cerebrovascular diseases; * Pregnant and lactating women; * Patients with cardiac arrhythmias; * Other conditions that the investigator considers ineligible for clinical trial.

Locations (1)

The Second Affiliated Hospital of Nanjing Medical University

Nanjing, Jiangsu, China

Outcomes

Primary Outcomes

Blood pressure measurement data

Systolic Pressure and Diastolic Pressure

Time frame: 30 minutes

Data from ClinicalTrials.gov

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