NCT04835857Recruiting
Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices
Comparison of Cuff-Less Wrist Wearable to Cuff Based Commercial Available Blood Pressure Measuring Devices in Health Volunteers With Normal or High Blood Pressure
Source: ClinicalTrials.gov · Last updated 5 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
(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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 91 (estimated)
- First submitted
- 5 Apr 2021
- Start date
- 1 Jan 2021
- Primary completion date
- 1 Jun 2026
- Lead sponsor
- Dynocardia, Inc
- Diseases
- High blood pressure
- NCT number
- NCT04835857
What you commit to
- Study type: Observational
- Planned participants: 91
- From 1 Jan 2021 to the primary completion date, 1 Jun 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior trauma or surgery at the radial artery monitoring site.
Other illness
- Any other condition that would increase the risk of participation in the study in the opinion of the site Investigator.
Other
- 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.
Who the study is looking for
- 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).
Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dynocardia Inc Coordinator of this site? Confirm its status | Newton | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.