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

Description

(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

Hypertension, Healthy

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Study Overview

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Study Details

Study overview

(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.

Comparison of Cuff-Less Wrist Wearable to Cuff Based Commercial Available Blood Pressure Measuring Devices in Health Volunteers With Normal or High Blood Pressure

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

Condition
Hypertension
Intervention / Treatment

-

Contacts and Locations

Newton

Dynocardia Inc, Newton, Massachusetts, United States, 02459

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * 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).
  • * Unable or unwilling to provide informed consent
  • * Any other condition that would increase the risk of participation in the study in the opinion of the site Investigator.
  • * 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.
  • * Prior trauma or surgery at the radial artery monitoring site.

Ages Eligible for Study

18 Years to 90 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Dynocardia, Inc,

Mohan Thanikachalam, MD, PRINCIPAL_INVESTIGATOR, Dynocardia, Inc

Study Record Dates

2025-12-21