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Artificial Intelligence in Echocardiography

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03936413
Recruitment Status : Withdrawn (This clinical trial will not be performed at CUIMC.)
First Posted : May 3, 2019
Last Update Posted : December 17, 2021
Sponsor:
Collaborator:
Caption Health, Inc.
Information provided by (Responsible Party):
Kerry Esquitin, New York Presbyterian Hospital

Brief Summary:
The goal of this study is to determine whether the Bay Labs artificial intelligence (AI) system can be used by minimally trained operators to obtain diagnostic quality echocardiographic images.

Condition or disease Intervention/treatment Phase
Cardiovascular Diseases Device: Bay Labs EchoGPS Echcoardiogram Device: Native Terason Echocardiogram Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: See protocol
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Artificial Intelligence in Echocardiography: a Pilot Study of Bay Labs Technology in Image Acquisition, Education, and Analysis
Estimated Study Start Date : January 13, 2020
Actual Primary Completion Date : January 13, 2020
Actual Study Completion Date : January 13, 2020

Arm Intervention/treatment
Experimental: Bay Labs EchoGPS group
In this arm, medical residents will use the Bay Labs EchoGPS system to perform an echocardiogram.
Device: Bay Labs EchoGPS Echcoardiogram
An echocardiogram will be performed in this arm using the Bay Labs EchoGPS. The Bay Labs EchoGPS system is an ultrasound system which uses the techniques of computer vision to analyze echocardiography images in real time. It then provides feedback to the user to optimize the images, and once they meet a specific level of quality it automatically records the images.

Active Comparator: Native Terason group
In this arm, medical residents will use the native Terason machine to perform an echocardiogram.
Device: Native Terason Echocardiogram
An echocardiogram will be performed in this arm using a native Terason echocardiography system. This system will not have any artificial intelligence assistance in image optimization or selection.




Primary Outcome Measures :
  1. Echocardiogram image acquisition quality [ Time Frame: immediately after the intervention ]

    Echocardiogram image acquisition quality. View quality will be characterized by the following system: adequate (American College of Emergency Physicians (ACEP) score 5), mildly limited (ACEP score 4), moderately limited (ACEP score 3), and severely limited (ACEP score 1 and 2). This will graded for each echocardiogram view as below and for the study as a whole.

    • Parasternal long axis
    • Parasternal short axis - aortic valve level
    • Parasternal short axis - mid ventricle
    • Apical 4 chamber
    • Apical 2 chamber
    • Subcostal - 4 chamber
    • Subcostal - inferior vena cava

  2. Educational outcome [ Time Frame: 1 month ]

    The medical resident's comfort with echocardiography will be established using the following questionnaire. The answers to each question are (1) very uncomfortable, (2) somewhat uncomfortable, (3) somewhat comfortable, and (4) very comfortable. These answers will be reported separately and in aggregate.

    How comfortable do you feel in your knowledge of the indications for ordering an echocardiogram? How comfortable do you feel in understanding echocardiographic reports as it applies to your patients? How comfortable do you feel in obtaining routine echocardiographic views using an ultrasound machine? How comfortable do you feel in interpreting echocardiographic images after the images have already been obtained? In an emergency situation, how comfortable would you feel in performing an echocardiogram using an ultrasound machine and interpreting the images to rule out serious cardiac pathology such as severe left ventricular systolic dysfunction or a large pericardial effusion?




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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients must be admitted to the resident cardiology ward service under a cardiology attending (general, heart failure, or private)
  • The patient must have either have undergone or be planned to undergo a formal echocardiogram within 1 day of the study echocardiogram
  • The patient must consent to the study
  • The patient's inpatient attending physician must give permission for the patient to be approached for consent

Exclusion Criteria:

  • Patient refusal
  • No recent or planned echocardiogram within 1 day of the study echocardiogram
  • Clinical need for an emergent echocardiogram that will immediately impact clinical decision making that should instead trigger obtaining a formal echocardiogram (for example, concern for cardiac tamponade or acute myocardial infarction).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03936413


Sponsors and Collaborators
New York Presbyterian Hospital
Caption Health, Inc.
Investigators
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Principal Investigator: Kerry A Esquitin, MD Columbia University
Publications:
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Responsible Party: Kerry Esquitin, Assistant Professor of Medicine, New York Presbyterian Hospital
ClinicalTrials.gov Identifier: NCT03936413    
Other Study ID Numbers: NYPresbyterianH
First Posted: May 3, 2019    Key Record Dates
Last Update Posted: December 17, 2021
Last Verified: December 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: Yes
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Kerry Esquitin, New York Presbyterian Hospital:
imaging
echocardiography
artificial intelligence
Additional relevant MeSH terms:
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Cardiovascular Diseases