CathEF: LVEF Prediction During ACS Using AI Algorithm Applied on Coronary Angiogram Videos

Sponsor
Montreal Heart Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05317286
Collaborator
Ottawa Heart Institute Research Corporation (Other)
240
1
21
11.4

Study Details

Study Description

Brief Summary

Left ventricular ejection fraction (LVEF) is one of the strongest predictors of mortality and morbidity in patients with acute coronary syndrome (ACS). Transthoracic echocardiography (TTE) remains the gold standard for LVEF measurement. Currently, LVEF can be estimated at the time of the coronary angiogram but requires a ventriculography. This latter is performed at the price of an increased amount of contrast media injected and puts the patients at risk for mechanical complications, ventricular arrhythmia or atrio-ventricular blocks. Artificial intelligence (AI) has previously been shown to be an accurate method for determining LVEF using different data sources. Fur the purpose of this study, we aim at validating prospectively an AI algorithm, called CathEF, for the prediction of real-time LVEF (AI-LVEF) compared to TTE-LVEF and ventriculography in patients undergoing coronary angiogram for ACS.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    240 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Prospective Validation of a Deep Learning Algorithm for Prediction of the Left Ventricular Ejection Fraction From Coronary Angiogram Videos in Patients With Acute Coronary Syndrome
    Actual Study Start Date :
    Jun 1, 2022
    Anticipated Primary Completion Date :
    Dec 31, 2022
    Anticipated Study Completion Date :
    Feb 29, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Area under the curve-Receiver Operating Characteristics (AUC-ROC) of the CathEF algorithm for differentiating a LVEF ≤ or >50%, compared to TTE-LVEF [Either 7 days before or up to 7 days after the coronary angiogram]

    Secondary Outcome Measures

    1. Comparing AUC-ROC of CathEF and ventriculography for differentiating a LVEF ≤ or >50% [Either 7 days before or up to 7 days after the coronary angiogram]

    2. Sensitivity of CathEF and ventriculography for differentiating a LVEF ≤ or >50% in comparison to TTE-LVEF. [Either 7 days before or up to 7 days after the coronary angiogram]

    3. Specificity of CathEF and ventriculography for differentiating a LVEF ≤ or >50% in comparison to TTE-LVEF. [Either 7 days before or up to 7 days after the coronary angiogram]

    4. Number of participants with major adverse cardiovascular events (Combined outcome of combined outcomeof mortality, ventricular arrhythmia requiring an intervention, heart failure, need for inotropic support, renal failure KDIGO≥2 and stroke) [At 7 days or before discharge, if earlier.]

    5. AUC-ROC of the re-trained CathEF algorthim for differentiating a LEVF ≤ or >50% [Either 7 days before or up to 7 days after the coronary angiogram]

    6. Sensitivity of the re-trained CathEF algorthim for differentiating a LEVF ≤ or >50% [Either 7 days before or up to 7 days after the coronary angiogram]

    7. Specificity of the re-trained CathEF algorthim for differentiating a LEVF ≤ or >50% [Either 7 days before or up to 7 days after the coronary angiogram]

    8. Likert scale on the impact on the procedure, ease of use and utility of the CathEF algorithm in the clinical practice, as assessed by interventional cardiologists [Through study completion, an average of 1 year.]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Informed consent signed by the participant

    • Acute coronary syndrome

    • Creatinine clearance ≥30 ml/min/m2 according to MDRD

    Exclusion Criteria:
    • Creatinine clearance <30 ml/min/m2 according to MDRD

    • No indication to perform TTE in the 7 days following coronary angiogram

    • Right bundle branch block

    • Suspected or confirmed left ventricular thrombus

    • Suspected or confirmed aortic dissection

    • Ventriculography not feasible

    • No left coronary system angiogram

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Robert Avram Montreal Quebec Canada H1T1C8

    Sponsors and Collaborators

    • Montreal Heart Institute
    • Ottawa Heart Institute Research Corporation

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Robert Avram, Principal Investigator, Montreal Heart Institute
    ClinicalTrials.gov Identifier:
    NCT05317286
    Other Study ID Numbers:
    • CathEF
    First Posted:
    Apr 7, 2022
    Last Update Posted:
    Aug 10, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Robert Avram, Principal Investigator, Montreal Heart Institute
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 10, 2022