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NCT04835857 · ClinicalTrials.gov registry record
Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices
A clinical trial of Healthy and Hypertension, sponsored by Dynocardia.
- Recruiting
- Registry status
- 91
- Enrollment target
- 1
- Study location
NCT04835857: Recruiting study of Healthy and Hypertension, sponsored by Dynocardia.
NCT04835857 is a study of Healthy and Hypertension that is actively recruiting participants, run by Dynocardia. The registered enrollment target is 91 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04835857, a study of Healthy and Hypertension, is actively recruiting participants, sponsored by Dynocardia.
- RECRUITING
- Registry status
- 91 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- DEVICE ViTrack
- DEVICE Oscillometric BP Device
- DEVICE Auscultatory cuff
Study Locations (1)
Massachusetts
- Dynocardia Inc - Newton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 91 participants |
| Start Date | 2021-01-01 |
| Est. Completion | 2026-11-30 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04835857
The ClinicalTrials.gov registry entry for NCT04835857 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 91 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (86% lower). The listed sponsor is Dynocardia, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Healthy appearing as the primary indexed condition, and to 3 interventions - of which ViTrack is the first listed.
NCT04835857 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT04835857 about?
NCT04835857 is a clinical study titled "Comparison of Cuff-Less Wrist Wearable Blood Pressure Device to Cuff Based Blood Pressure Measuring Devices". (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.
What is the current status of trial NCT04835857?
This trial is currently recruiting. The enrollment target is 91 participants. The study started on 2021-01-01. Estimated completion is 2026-11-30.
What conditions does trial NCT04835857 study?
This clinical trial studies the following conditions: Healthy, Hypertension.
What interventions are being tested in trial NCT04835857?
The interventions under investigation include: ViTrack (DEVICE), Oscillometric BP Device (DEVICE), Auscultatory cuff (DEVICE).
Who is sponsoring clinical trial NCT04835857?
This trial is sponsored by Dynocardia, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04835857 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.