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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04931264
Other study ID # YUWELL-YLQX202101
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2021
Est. completion date March 8, 2022

Study information

Verified date March 2022
Source The Second Hospital of Nanjing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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).


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date March 8, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
YuWell YE660D Electronic Sphygmomanometer
Measurement blood pressure by YuWell YE660D Electronic Sphygmomanometer and Desk Mercury Sphygmomanometer

Locations

Country Name City State
China The Second Affiliated Hospital of Nanjing Medical University Nanjing Jiangsu

Sponsors (2)

Lead Sponsor Collaborator
The Second Hospital of Nanjing Medical University Jiangsu Yuyue medical equipment & supply Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood pressure measurement data Systolic Pressure and Diastolic Pressure 30 minutes
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