Vital Signs Blood Pressure Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cardiovascular Diseases
- Sponsor
- Stanford University
- Enrollment
- 50
- Primary Endpoint
- Collection of Subject Height
- Status
- Not yet recruiting
- Last Updated
- 8 days ago
Overview
Brief Summary
The purpose of this study is collect subject vitals with a blood pressure cuff, electrocardiogram (ECG), and photoplethysmogram (PPG). This data can then be used to develop a reliable, accurate, noninvasive, and continuous blood pressure monitoring device.
Investigators
Alexandra Ruan
Principal Investigator
Stanford University
Eligibility Criteria
Inclusion Criteria
- •Age \>17 and \<65 years
- •BMI \>20 and \<35
Exclusion Criteria
- •Age \<18 or \>64
- •BMI \<20 or \>35
- •Pregnancy
Outcomes
Primary Outcomes
Collection of Subject Height
Time Frame: Less than 1 minute
Height in meters
Collection of Subject Age
Time Frame: Less than 1 minute
Age in years
Collection of ECG Waveforms
Time Frame: 5 minutes
Using an electrocardiogram (ECG) to measure heart rhythm
Systolic and Diastolic Blood Pressure Measurement
Time Frame: 1-2 minutes
Using blood pressure cuff; measured three times to find the initial, interim, and final blood pressure
Collection of Subject Name (optional)
Time Frame: Less than 1 minute
Collection of Subject Weight
Time Frame: Less than 1 minute
Weight in kilograms
Collection of PPG Waveforms
Time Frame: 5 minutes
Using a photoplethysmography (PPG) to monitor heart rate
Collection of Subject Medical Comorbidities
Time Frame: 1 minute