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imPulse™ Una Full-spectrum, Over Clothing E-stethoscope

NCT04556149 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 34

Last updated 2020-12-21

No results posted yet for this study

Summary

This study generates robust clinical data to train ML/AI algorithms of the Sponsor's imPulse™ Una full-spectrum e-stethoscope for digital diagnostic feature synthesis of symptomatic SARS-CoV-2/COVID-19 biosignatures for rapid and accurate mass screening.

Conditions

  • Corona Virus Infection
  • Coronavirus

Interventions

DEVICE

imPulse™ Una e-stethoscope

The imPulse™ System is an every/anywhere-point-of-care cardiopulmonary functional state assessment platform designed to capture normal and abnormal, audible and inaudible cardiopulmonary sounds, rhythms and patterns, via a real-time, intelligent, full-spectrum phonocardiogram obtained from direct to skin coupling or through a layer of clothing.

DEVICE

Philips Lumify Ultrasound System

Point-of-care ultrasound

Sponsors & Collaborators

Principal Investigators

  • Kelly Dooley, MD, PhD · Johns Hopkins School of Medicine

  • Ed Fuchs, MBA · Johns Hopkins School of Medicine

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-10-01
Primary Completion
2020-12-02
Completion
2020-12-02

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT04556149 on ClinicalTrials.gov