Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT04024566

Rapid Non-invasive Detection of Aortic Stenosis

Aortic Stenosis Screening Using the Avicena Vivio System

Status
Withdrawn
Phase
Study type
Observational
Enrollment
0 (actual)
Sponsor
Avicena LLC · Industry
Sex
All
Age
60 Years – 95 Years
Healthy volunteers

Summary

Avicena is developing new non-invasive methods (hardware and software) for diagnosis of a variety of heart conditions. This study is designed to compare data obtained using Avicena's device, the Vivio, to data obtained from transthoracic echocardiography (TTE) for the diagnosis of moderate-to-severe aortic stenosis. Aortic stenosis (AS) is a disease of the valve (aortic valve) that separates the left ventricle of the heart from the aorta. When AS is severe, the heart cannot pump adequate amounts of blood into the arterial tree. AS is often silent until the disease is severe. This study compares a rapid test using Vivio to a longer and more expensive test that is the current gold standard for diagnosis of AS, TTE.

Detailed description

The study proposed here is a research study to develop the Vivio system for diagnosis of severe AS. The data gathered in this study will be used to optimize the Avicena software algorithm used to make the diagnosis of AS. The Vivio device is an optical-type tonometer that operates based on capturing the vibrations of the skin due to the arterial pulse pressure wave as it propagates through the underlying carotid vessel. When applied to the neck over the subject's carotid pulse, an arterial waveform (pressure tracing) and heart sounds are sensed, and sent to an iPad using Bluetooth, then sent to Avicena for analysis. After informed consent subjects will undergo a brief cardiac-focused history and examination. All subjects will have bilateral exams with the Vivio (\~5 minutes each) conducted by a study doctor or nurse, and a standard clinical resting TTE conducted by a certified technician. The entire study visit should take 1.5 hours, and there is no follow up.

Conditions

Interventions

TypeNameDescription
DEVICEVivio SystemOptical/sensor tonometer applied to the neck over the carotid pulse (bilateral)

Timeline

Start date
2019-08-14
Primary completion
2022-07-18
Completion
2022-07-18
First posted
2019-07-18
Last updated
2022-07-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04024566. Inclusion in this directory is not an endorsement.