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Testing Automated Echocardiography

NCT04943965 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2023-10-19

No results posted yet for this study

Summary

The purpose of this research is to determine if software can accurately predict certain heart parameters from chest wall ultrasound (non-radiation, non-invasive, imaging modality). An approved ultrasound device (Lumify) will be used to obtain images prior to cardiac surgery.

Conditions

  • This Study is Being Conducted to Collect Echocardiographic Data to Test the Lumify Ultrasound With Hemodynamic Automation Device

Interventions

DIAGNOSTIC_TEST

Ultrasound imaging

The intervention is non-invasive, chest wall, echocardiographic image acquisition in the cardiac operating room prior to a scheduled cardiac surgery. Echocardiographic images will be taken at three, key, timepoints in the operating room prior to cardiac surgery: 1. Pre-induction. 2. Post-induction / Pre-PAC 3. Post-induction / Post-PAC

Sponsors & Collaborators

Principal Investigators

  • Roderic G Eckenhoff, MD · University of Pennsylvania, Department of Anesthesiology and Critical Care

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-11
Primary Completion
2022-06-07
Completion
2023-10-03
FDA Device
Yes

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 NCT04943965 on ClinicalTrials.gov