No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 90
Sex
Any
Study type
Observational
Participants needed
91 (estimated)
Sponsor
Dynocardia, Inc · Industry
Who this trial is looking for
This trial is looking for healthy adults aged 18 and older to compare a new wrist blood pressure device with standard cuff devices. Participants need to provide consent and meet certain health criteria to join.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I am healthy or have high blood pressure.
I can understand and sign consent forms.
I agree to participate in the study.
You may not be able to join if
I cannot provide informed consent.
I have a medical condition that makes participation risky.
My blood pressure is very different between my arms.
I have had surgery or trauma at my wrist area.
I experience pain or distortion in my wrist.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed 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.
Trial Locations
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Status
Eligibility Criteria
Inclusion 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 perfor…
Inclusion 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).
Exclusion Criteria:
* 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.
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