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Relevance of Artificial Intelligence-Assisted Echocardiography for Left Ventricular Ejection Fraction Assessment in Geriatric Patients (REFERENCE-AI)

27. juli 2026 opdateret af: Gérond'if

Heart failure (HF) is the leading cause of hospitalization among adults aged 80 years and older and represents a major diagnostic challenge in geriatric medicine due to frequently atypical clinical presentations and the presence of multiple comorbidities. Although transthoracic echocardiography (TTE) with measurement of left ventricular ejection fraction (LVEF) remains the gold standard for cardiac functional assessment, access to echocardiography is often limited in geriatric wards.

Recent advances in artificial intelligence (AI) have enabled the development of portable ultrasound devices and automated image analysis software capable of providing reliable and reproducible LVEF measurements. AI-assisted automated LVEF assessment (AutoEF-AI) may therefore represent a valuable alternative to conventional echocardiography for the cardiac evaluation of older patients with heart failure.

Studieoversigt

Detaljeret beskrivelse

Prospective, single-center interventional study comparing two methods of left ventricular ejection fraction measurement in patients aged 75 years and older hospitalized for acute heart failure.Each hemodynamically stable participant will undergo two echocardiographic examinations performed within 24 hours:

  • Standard Echocardiography (Reference Method)
  • AI-assisted automated LVEF assessment (AutoEF-AI)

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

130

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

      • Paris, Frankrig, 75013
        • Rekruttering
        • Broca Hospital
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Age ≥75 years.
  • Hospitalization in a geriatric unit for acute heart failure according to the 2021 ESC diagnostic criteria.
  • Hemodynamic stability at the time of echocardiographic examination.
  • Ability to understand study information, provide written informed consent, and willingness to participate.
  • Affiliation with, or beneficiary of, a health insurance/social security scheme.

Exclusion Criteria:

  • Hemodynamic instability preventing echocardiographic assessment.
  • Contraindication to transthoracic echocardiography.
  • Patients under legal protection (guardianship, curatorship, or judicial protection measures) or unable to provide informed consent.
  • Refusal to participate in the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Diagnostisk
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Andet: Standard Echocardiography (Reference method)
The standard echocardiography will be performed by a cardiologist as part of routine clinical care.
The standard echocardiography will be performed by an expert cardiologist as part of routine clinical care and will serve as the gold standard
Eksperimentel: AutoEF-AI Assessment
AI-assisted automated LVEF assessment

Performed by a geriatrician who has completed a one-day practical training session and combines:

  • A handheld ultrasound device providing real-time image acquisition guidance for obtaining apical views.
  • Us2.ai software for automated LVEF analysis. The geriatrician is blinded to results of the gold standard echocardiography performed by the cardiologist.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Agreement between LVEF measured using AutoEF-AI and LVEF measured using standard echocardiography.
Tidsramme: At baseline

Agreement will be assessed using:

  • Intraclass Correlation Coefficient (ICC)
  • Spearman correlation coefficient
  • Bland-Altman analysis
  • Weighted kappa coefficient for the classification of patients according to LVEF categories (≤40%, 41-49%, and ≥50%)
At baseline

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Diagnostic performance of AutoEF-AI for the detection of LVEF <50%, including sensitivity, specificity, positive predictive value, negative predictive value, and overall accuracy.
Tidsramme: At baseline
Calculation of the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and overall accuracy of AutoEF-AI for identifying left ventricular ejection fraction (LVEF) below 50%, compared with the standard reference method.
At baseline
Analysis of factors associated with agreement between the two methods
Tidsramme: At baseline
Multiple linear regression model will be used to identify clinical and technical variables (age, sex, cardiovascular history, presence of a pacemaker, cardiac arrhythmias, image quality, comorbidities, etc.) associated with a significant discrepancy between LVEF measurements obtained using AutoEF-AI and standard echocardiography.
At baseline
Feasibility of AutoEF-AI use by a geriatrician after a short training program
Tidsramme: At baseline
  • Success rate of valid image acquisition (i.e acquizition of analyzable apical views suitable for automated analysis)
  • Quality of the acquired images (image quality score and proportion of non-analyzable images)
  • Difficulties encountered during the use of the AutoEF-AI device
At baseline

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Efterforskere

  • Ledende efterforsker: Olivier HANON, MD PhD, Geriatric Department, Broca hospital

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

7. juli 2026

Primær færdiggørelse (Anslået)

30. juni 2028

Studieafslutning (Anslået)

30. juni 2028

Datoer for studieregistrering

Først indsendt

1. juli 2026

Først indsendt, der opfyldte QC-kriterier

8. juli 2026

Først opslået (Faktiske)

14. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

28. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

27. juli 2026

Sidst verificeret

1. juli 2026

Mere information

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