Clinical Trial of YuWell YE900 Electronic Sphygmomanometer
Not Applicable
Completed
- Conditions
- Blood Pressure
- Interventions
- Diagnostic Test: YuWell YE900 Electronic Sphygmomanometer
- Registration Number
- NCT04379323
- Lead Sponsor
- The Second Hospital of Nanjing Medical University
- Brief 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).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 92
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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description YuWell YE900 and mercury sphygmomanometer YuWell YE900 Electronic Sphygmomanometer Blood Pressure Measurement with the YuWell YE900 Electronic Sphygmomanometer (YuWell YE900) and with Desk Mercury Sphygmomanometer.
- Primary Outcome Measures
Name Time Method Blood pressure measurement data 30 minutes Systolic Pressure and Diastolic Pressure
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
The Second Affiliated Hospital of Nanjing Medical University
🇨🇳Nanjing, Jiangsu, China