Avicena LVDP Validation Study in Healthy Volunteers

NCT05673174 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 321

Last updated 2023-01-06

No results posted yet for this study

Summary

The purpose of this study is to document the utility of the Vivio System in quantifying LVDP in healthy volunteers.

Conditions

  • Healthy

Interventions

DIAGNOSTIC_TEST

Non-Invasive Estimation of Left Ventricular Diastolic Pressure

Modified blood pressure cuff used to detect arterial waveforms used for the estimation of LVDP

Sponsors & Collaborators

  • Avicena LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-06-16
Primary Completion
2022-08-30
Completion
2022-08-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05673174 on ClinicalTrials.gov