None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Volunteers at least 20 years of age and less than 80 years of age 2) Those who voluntarily decide to participate in this clinical trial and give written consent in the informed consent form 3) Those who meet the selection and conditions (blood pressure, arm circumference) of 4.2.4.6.4 of 'Medical Device Standard - Annex 2 - 43. Automatic Electronic Blood Pressure' of KFDA
Exclusion criteria
Exclusion criteria: 1) Hypovolemia or similar conditions and circumstances are likely to prevent blood pressure from remaining constant for approximately 1 hour 2) Administration of short-acting vasoactive agents or similar medications is likely to prevent blood pressure from remaining constant for approximately 1 hour 3) Allergic to nylon (cuff material) 4) Have a diagnosed arrhythmia 5) If not more than 30 minutes after ate foods. 6) If not more than one hour after drinking coffee or not more than 15 minutes after smoking 7) Have exercised immediately before blood pressure measurement 8) Are otherwise unable to participate in this study in the opinion of the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Difference in systolic blood pressure and difference in diastolic blood pressure measured with an automated electronic sphygmomanometer (MBP100U) and an aneroid sphygmomanometer, respectively. | — |
Secondary
| Measure | Time frame |
|---|---|
| The average of the differences between the measured systolic blood pressure and the differences between the measured diastolic blood pressure ;The standard deviation (SD) of the differences between the measured systolic blood pressure and the differences between the measured diastolic blood pressure | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center