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Heart FailureELEGANTNCT06968533

ECG Low Ejection Fraction Detection and Guiding in AI Navigated Treatment Era

A study testing AI-ECG guided diagnosis in people with Heart Failure and Ventricular Dysfunction, Left, run by National Defense Medical Center, Taiwan at 1 site in Taiwan.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Asymptomatic left ventricular systolic dysfunction (ALVSD), identified as a key component of stage B heart failure (HF) by AHA/ACC guidelines, is a common precursor to clinically overt HF. Read more about this study

Who is it for?
Ages 60 to 85 yearsHealthy volunteers can take part
What is being tested?
AI-ECG guided diagnosis
Could I receive a placebo?
No, everyone receives an active treatment
How many people
13,350 participants
Where
1 siteTaiwan
Study dates
1 Jun 2024to 1 Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 to 85 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Outpatients with at least one 12-lead ECG
  • Age between 60-85 years

Who cannot join

  • Documented echocardiography within the previous 6 months
  • Known severe LV dysfunction (LVEF <40%)
  • Known heart failure history
  • Scheduled echocardiography exam

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Taiwan1 site
  • Tri-Service General Hospital, National Defense Medical Center

    Taipei, 11490

Other trials in Taiwan

About this study

Official title: ECG Low Ejection Fraction Detection and Guiding in AI Navigated Treatment Era (ELEGANT): A Randomized Control Trial

Asymptomatic left ventricular systolic dysfunction (ALVSD), identified as a key component of stage B heart failure (HF) by AHA/ACC guidelines, is a common precursor to clinically overt HF. This progressive chronic disease affects over 23 million people worldwide and leads to significant morbidity, mortality, and healthcare costs. Although ALVSD presents a relatively lower risk compared to symptomatic reduced ejection fraction HF, it remains associated with a 1.6-fold increase in the risk of incident HF, a 2.13-fold increase in cardiovascular mortality, and a 1.46-fold increase in all-cause mortality. The prevalence of ALVSD ranges from 3% to 6%, at least twice that of symptomatic HF. To prevent progression to symptomatic heart failure and associated morbidities and mortalities, guideline-directed medical therapy, including ACEIs/ARBs or beta-blockers, is essential for patients with ALVSD. However, distinguishing individuals with ALVSD from the general population is challenging due to the lack of symptoms. Effective screening methods are crucial to identify individuals with ALVSD. Traditionally, diagnosing ALVSD involves screening asymptomatic populations using transthoracic echocardiography (TTE), which is costly, time-consuming, and inconvenient for patients. Other screening methods, such as laboratory tests for brain natriuretic peptide (BNP) or N- terminal pro-atrial natriuretic peptide (NT-proBNP), have insufficient diagnostic performance.

Previous research proposed an AI-based alarm system (AI-S) to screen patients for ALVSD, demonstrating greater accuracy than BNP screening and improved accessibility compared to widespread echocardiography. AI-S demonstrated a sensitivity of 92.6% (standard error [SE] 0.042) for detecting medium-risk ALVSD patients and 63% (SE 0.154) for high-risk ALVSD patients, with a specificity of 92.7% (SE 0.003) for medium-risk patients and 98.7% (SE 0.002) for high-risk patients. AI-S is accuracy, noninvasive, highly accessible in local medical clinics, less time-consuming, and cost-effective, making it a valuable screening tool for identifying ALVSD prior to echocardiography or other confirmatory diagnostic methods.

To date, no randomized controlled trial has assessed the cost-effectiveness and impact of AI-assisted screening tools for heart failure prevention in Asians. The ECG AI-Guided Screening for Low Ejection Fraction (EAGLE) trial reported a 32% increase in diagnosing of low left ventricular ejection fraction (defined as LVEF ≤50%) within 90 days of the ECG. However, this population was not Asian, and randomization involved primary care teams rather than participants. Therefore, this randomized controlled trial is designed to evaluate the impact of AI-S on diagnosing low ejection fraction in Asians, its cost-effectiveness, and the incidence of worsening HF (defined as admission for HF or HF-related emergency department visits).

Being tested
AI-ECG guided diagnosis
Keywords
Left ventricular dysfunction, artificial intelligence, Electrocardiography
Medical subject headings
Heart Failure, Ventricular Dysfunction, Left, Disease, Asymptomatic Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AI-ECG guided diagnosisDiagnostic test

    Participants undergo screening using the AI-ECG system. Participants identified as medium- to high-risk for LV dysfunction (LVEF <50%) are recommended for echocardiography to confirm the diagnosis and guide subsequent management.

Study groups in NCT06968533
Study groupRoleWhat they receive
AI-ECG guided diagnosisExperimentalParticipants undergo screening using the AI-ECG system. Participants identified as medium- to high-risk for LV dysfunction (LVEF <50%) are recommended for echocardiography to confirm the diagnosis and guide subsequent management.
Receives: Diagnostic Test: AI-ECG guided diagnosis
Standard clinical careNo interventionParticipants undergo screening using the AI-ECG system, but diagnosis and management follow usual clinical practice without immediate echocardiography based on AI-ECG results.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Detection of mildly reduced or severely reduced LV function

    The endpoint measures the proportion of participants with mildly reduced (LVEF 40-49%) or severely reduced (LVEF <40%) LV function detected by echocardiography.

    Measured: Within 90 days after randomization

Secondary outcomes (3)
  1. Severe reduced LVEF

    The endpoint measures the proportion of participants with severely reduced LV function (LVEF <40%) identified by echocardiography.

    Measured: Within 90 days after randomization

  2. Heart failure events

    The endpoint measures the composite number of heart failure emergency department visits and heart failure admissions.

    Measured: Within 90 days after randomization

  3. Receiving echocardiography exam

    The endpoint measures the proportion of participants who receive echocardiography examination.

    Measured: Within 90 days after randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 May 2025
  2. Study start1 Jun 2024
  3. Primary completion1 Jun 2027 (estimated)
  4. Study completion1 Jun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Screening
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
13,350 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06968533
Sponsor's protocol ID
TSGHA25002
Acronym
ELEGANT
Status last verified
May 2025
First submitted
5 May 2025
Last updated
21 May 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing AI-ECG guided diagnosis in people with Heart Failure and Ventricular Dysfunction, Left, run by National Defense Medical Center, Taiwan at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 21 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Detection of mildly reduced or severely reduced LV function (time frame: Within 90 days after randomization). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 May 2025.

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