hypertension
Conditions
Interventions
experimental group:An arm-type electronic sphygmomanometer was utilized to measure the systolic blood pressure, diastolic blood pressure, and pulse rate of the subjects. Each subject underwent three m
control group:An electronic sphygmomanometer (Omron) was employed to measure the systolic blood pressure, diastolic blood pressure, and pulse rate of the subjects. Each subject underwent three measure
control group:A desktop sphygmomanometer equipped with a dual earpiece stethoscope was utilized to measure the subjects' systolic blood pressure, diastolic blood pressure, and pulse rate. Each subject
Sponsors
Jiangsu Shengze Hospital (Single Center)
Eligibility
Sex/Gender
All
Age
14 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1 Participants aged between 14 and 85 years; 2 Individuals not engaged in other clinical evaluations within the preceding week; 3 Participants must demonstrate good compliance and voluntarily agree to partake in this evaluation; 4 Criteria for blood pressure and pulse rate of clinical trial subjects: 1) Blood pressure requirements: 5% of subjects must have a systolic blood pressure lower than 100 mmHg; 5% must have a systolic blood pressure exceeding 160 mmHg; 20% must have a systolic blood pressure greater than 140 mmHg; 5% must have a diastolic blood pressure below 60 mmHg; 5% must have a diastolic blood pressure above 100 mmHg; 20% must have a diastolic blood pressure exceeding 85 mmHg, with the remaining subjects distributed between these limit values. 2) Pulse rate range and distribution: 40-180 beats per minute.
Exclusion criteria
Exclusion criteria: 1. Individuals with mental disorders; 2. Individuals with severe cardiac and hepatic diseases; 3. Individuals with renal failure or significant arrhythmias; 4. Individuals considered unsuitable for participation by clinical trial staff.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| systolic pressure;diastolic pressure;Pulse rate; | — |
Countries
China
Contacts
Public ContactZhiqiang Qi
Jiangsu Shengze Hospital
Outcome results
None listed