Clinical trial Recruiting at 1 site Observational Ages 18 to 85

AI-assisted echocardiography to predict outcomes in left atrial cardiomyopathy

Official title: Evaluation of Artificial Intelligence-Assisted Echocardiography (AI-echo) in the Early Diagnosis and Prognostic Stratification of Left Atrial Cardiomyopathy (LACM) in Patients With Acute Cardiac Disease

Run by University of Calabria · NCT07009639 · Data updated 2026-11-12

This will try whether AI-assisted echocardiography speeds up atrial strain measurements and whether those strain changes help predict atrial fibrillation and in-hospital complications in adults in a cardiac care unit.

More Atrial Cardiomyopathy trials

Quick facts

Study typeObservational
Ages18 Years to 85 Years
SexAll
Enrollment45 (estimated)
SponsorUniversity of Calabria
Academic / other
Locations1 site (Cosenza)
StatusRecruiting
StartedJuly 1, 2025
Main results expectedSeptember 1, 2025
Study endsNovember 30, 2025
Registry record updatedAugust 11, 2025
Trial IDNCT07009639 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–85 hospitalized in the coronary/cardiac care unit for acute cardiac problems and able to provide written informed consent are the ideal candidates.

Probably not a fit

Patients who are severely hemodynamically unstable, have a very poor echocardiographic window, cannot continue or refuse consent, or are not admitted to the CCU are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational, single-center study will compare the time needed to obtain atrial strain measurements using AI-assisted echocardiography versus conventional methods in patients hospitalized in the cardiac care unit. Investigators will record LASr, LASct, and LAScd parameters and track the onset of atrial fibrillation and in-hospital adverse outcomes, adjusting analyses for comorbidities and standard echocardiographic variables. The primary endpoints are reduction in analysis time with AI-echo and the association between strain changes and AF, complications, or mortality during hospitalization. Adult patients (18–85) admitted for acute cardiac conditions who can give written consent will be enrolled at the Annunziata Hospital (Cosenza, Italy).

Why it matters

Potential benefit: If successful, AI-echo could provide faster and more consistent atrial strain readings that help clinicians identify patients at higher risk of AF or complications sooner.

How similar studies have gone: Atrial strain is an established marker of left atrial disease and prior work shows AI can speed echocardiographic analysis, but applying AI-echo for in-hospital prognostic prediction is still relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age between 18 and 85 years.
2. Hospitalization in CCU for acute cardiac pathology (e.g. acute coronary syndrome, acute or exacerbated heart failure, malignant arrhythmias, etc.).
3. Ability to provide written informed consent.

Exclusion Criteria:

1. Severe hemodynamic instability, history to contraindicate the execution of the echocardiographic examination.
2. Severely inadequate echocardiographic window that precludes atrial or ventricular morpho-functional assessment.
3. Inability to continue the study for clinical reasons, logistics or patient refusal.

Where it's running

  • "Annunziata" Hospital
    Cosenza, Italy
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.