Clinical Trial of YuWell YE900 Electronic Sphygmomanometer

  • STATUS
    Recruiting
  • participants needed
    85
  • sponsor
    The Second Hospital of Nanjing Medical University
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Updated on 5 August 2020
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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).

Details
Condition Blood Pressure, Blood pressure
Age 3years - 100years
Treatment YuWell YE900 Electronic Sphygmomanometer
Clinical Study IdentifierNCT04379323
SponsorThe Second Hospital of Nanjing Medical University
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

3 Years and older (Child, Adult, Older Adult)
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
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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