Compares a wrist-worn blood pressure device with cuff devices
Compares a wrist device with cuff devices in healthy adults.
Key facts
- Who runs it
- Dynocardia, Inc
- Where
- Newton, United StatesSee the site
- Trial code
- Registry title
- Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices
- Status
- Recruiting
- People taking part
- 91 people, planned
- Started
- 1 Jan 2021
- Expected to end
- 30 Nov 2026
- Type of study
- Observational
- Treatments tested
- ViTrack
- Oscillometric BP Device
- Auscultatory cuff
- Record updated
- 5 September 2025
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for healthy adult volunteers with normal or high blood pressure. It compares a cuff-less wrist device with standard cuff blood pressure devices.
- Age
- 18 years and above (up to 90 years)
- Sex
- All sexes; the trial wants equal numbers of men and women
- Disease stage
- Healthy volunteers with normal or high blood pressure, with a regular heart rhythm (sinus rhythm)
Main reasons for not taking part
- Cannot or does not want to give informed consent
- More than 10 mm Hg difference in top blood pressure between the left and right arm
- Dialysis shunt in the upper arm or forearm
- Wrist deformity or wrist pain from arthritis
- Earlier injury or surgery at the wrist artery measuring site
This trial only enrols healthy participants. The registry sentence this rests on: Health volunteers 18 years and above; equal numbers of males and females to address Sex As a Biological Variable (SABV); and in sinus rhythm.
The registry criteria, word for word
Show all 9 criteriaShow less
Who can take part
- Health volunteers 18 years and above; equal numbers of males and females to address Sex As a Biological Variable (SABV); and in sinus rhythm
- Agree to commit to participate in the current protocol
- Provide written informed consent prior to any study procedures being performed (all subjects should be able to understand the informed consent form and any other documents that subjects are required to read)
Who cannot take part
- Prior trauma or surgery at the radial artery monitoring site
- Any other condition that would increase the risk of participation in the study in the opinion of the site Investigator
- Unable or unwilling to provide informed consent
- A difference of >10 mm Hg in left versus right arm oscillometric systolic BP
- Upper extremity arteriovenous hemodialysis shunt
- Wrist distortion or pain from arthritis
Check if you might fit
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 90 years old?
Where in United States
- Dynocardia IncNewton, United StatesContact: Gokul RajamanickamTaking people
About the trial
What the trial wants to find out
(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.
The group in the trial
- Experimental-Arm
For the same subject, 1. ViTrack wrist cuff is applied on one of the wrist 2. Standard Oscillometric cuff is applied to the brachial artery / wrist of the same arm 3. Auscultatory cuff is applied to the brachial artery of the same arm
Treatment: ViTrack, Oscillometric BP Device, and Auscultatory cuff
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Comparison of Cuff-Less Wrist Wearable to Cuff Based Commercial Available Blood Pressure Measuring Devices in Health Volunteers With Normal or High Blood Pressure
- Plain-language title
- Compares a wrist-worn blood pressure device with cuff devicesGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Fit questions
- Built from NCT04835857, who can take part
- Record updated
- 5 September 2025