hypertension
Conditions
Sponsors
Zhongshan Hospital, Fudan University; Fenglin Community Health Service Center, Xuhui District, Shanghai
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: 1. People over the age of 18 who need to monitor their blood pressure; 2. Not participating in other clinical trials within one week; 3. Good compliance, voluntary participation in this trial, and signed written informed consent.
Exclusion criteria
Exclusion criteria: 1. Rashes or wounds on the chest or arms of subjects with difficulty in measuring blood pressure due to skin causes; 2. Women who are pregnant at the time of participation in the study; 3. Subjects implanted with pacemakers or defibrillators; 4. Subjects who have difficulty measuring blood pressure in a seated position; 5. Subjects with arteriovenous shunt or endovascular access on either arm; 6. Subject suffers from any form of arrhythmia symptoms; 7. Subject has disease of vascular stenosis; 8. Subjects who have not signed the informed consent form or are considered inappropriate by the investigator to participate in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The accuracy of Blood Pressure value measurement; | — |
Countries
China
Contacts
Public ContactHong Jiang, Bihua Chen
Department of Cardiology, Zhongshan Hospital, Fudan University; Fenglin Community Health Service Center, Xuhui District, Shanghai
Outcome results
None listed