Actively Recruiting
Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices
Led by Dynocardia, Inc · Updated on 2025-09-05
91
Participants Needed
1
Research Sites
308 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
(1) To compare cuff-less wrist wearable radial artery blood pressure measurements utilizing ViTrack(developed by Dynocardia) to the cuff based commercially available blood pressure device, in healthy volunteers with normal or high blood pressure.
CONDITIONS
Official Title
Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy volunteers aged 18 years and above
- Equal numbers of males and females to address Sex As a Biological Variable (SABV)
- Participants must be in sinus rhythm
- Agree to participate in the study
- Provide written informed consent before any study procedures
You will not qualify if you...
- Unable or unwilling to provide informed consent
- Any condition increasing risk of participation as judged by the investigator
- Difference greater than 10 mm Hg between left and right arm systolic blood pressure
- Presence of upper extremity arteriovenous hemodialysis shunt
- Wrist deformity or pain due to arthritis
- Prior trauma or surgery at the radial artery monitoring site
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Dynocardia Inc
Newton, Massachusetts, United States, 02459
Actively Recruiting
Research Team
M
Mohan Thanikachalam, MD
CONTACT
G
Gokul Prasath Rajamanickam, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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