A study to improve the accuracy of Blood Pressure data of Valencell Finger clip and watch using standard method.
- Conditions
- Health Condition 1: R688- Other general symptoms and signs
- Registration Number
- CTRI/2024/01/062053
- Lead Sponsor
- Valencell, Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Participants must be able to provide an informed consent or have legally authorized representative consent to participate.
2.Participant must be willing and able to comply with the study procedures.
3.Participant must be = 18 years of age.
4.Participants with a upper arm circumference in the range of the reference cuff
5.Participants who fit in one of the following categories with a goal of 15% minimum in each and up to 15% can fall outside of these categories:
a.Age Group 18-30: Any BP systolic over 140 mmHg.
b.Age Group 18-30: Overweight(BMI >25) with BP systolic under 100 mmHg.
c.Age Group 30+: Any with BP systolic over 160 mmHg.
d.Age Group 30+: Any with BP systolic under 100 mmHg.
e.Age Group 18+: With any BP.
• Lack of Informed consent.
• Participants with deformities or abnormalities that may prevent proper application of the device under test.
• Participant is evaluated by the investigator or clinician and found to be medically unsuitable for participation in this study.
• Participants with known heart dysrhythmias.
• Participants with compromised circulation or peripheral vascular disease.
• Participants who are pregnant and/or lactating.
• Participants who cannot tolerate sitting for up to 30 minutes.
• Participant falls into a category that has already been filled
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method