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Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices

NCT04835857

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

(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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Hypertension
  • Healthy

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 to 90 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Dynocardia, Inc
Last updated on ClinicalTrials.gov
September 5, 2025

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Massachusetts · 1

  • Dynocardia Inc · Newton, MA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.