hypertension
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.agree to participate in this clinical study; 2.aged 3-80 years old; 3.able to understand the purpose of the study and voluntarily sign the informed consent.
Exclusion criteria
Exclusion criteria: 1.Subjects who do not possess normal behavioral understanding and control; 2.Subjects with severe bleeding tendency or sickle cell personnel; 3.Subjects with skin damage at the measurement site; 4.Subjects with intravenous fluids or catheters in the measuring limb; 5.Pregnant or lactating females; 6.Subjects who, in the opinion of the investigator, are unable to follow the study protocol or who, for either reason, are deemed unfit to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| blood pressure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of Device Defects;Incidence of Adverse Events; | — |
Countries
China
Contacts
Feidong People's Hospital