ClinicalTrials.gg
Not yet recruitingNCT07038018Updated Jun 26, 2025

External Validation of Artificial Intelligence-enabled Electrocardiography (AI-ECG) for the Detection of Left Ventricular Dysfunction (LVD)

An observational study in Cardiac Disease, sponsored by Tri-Service General Hospital. Not yet recruiting at 13 sites in Taiwan. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2025-06-26.

Primary conditionVentricular Dysfunction, LeftRegistry: Heart DiseasesReclassifiedWhy we changed it
Registry
Heart Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Ventricular Dysfunction, Left
Why
  1. The study's title name Ventricular Dysfunction, Left, a narrower term within Heart Diseases.
Confidence
High: the new condition is named in the study's own title. Of 46 hand-checked studies reclassified this way, 72% were exactly right and 89% in the right disease family; the registry's first term was right for 4% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Tri-Service General Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 2 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
12,500
Ages
18 Years to 100 Years
Sex
All
01

Study summary

This is a multi-center, retrospective study evaluating the performance of an artificial intelligence-enabled electrocardiography (AI-ECG) algorithm in detecting reduced left ventricular ejection fraction (LVEF ≤ 40%). All included patients from participating hospitals must have undergone a digital 12-lead electrocardiogram (ECG) and an echocardiogram with assessment of LVEF within seven days. The AI-ECG algorithm will be applied to evaluate its diagnostic performance, which will be further assessed across subgroups stratified by demographic characteristics and clinical factors.

Read the detailed description

Data were collected from 13 hospitals, excluding the medical center that developed the artificial intelligence-enabled electrocardiography (AI-ECG) algorithm. The primary objective of the study was to evaluate the sensitivity and specificity of the AI-ECG model in detecting left ventricular dysfunction, defined as left ventricular ejection fraction (LVEF) ≤ 40%. To ensure clinical applicability, predefined thresholds required both sensitivity and specificity to exceed 0.80 in external validation cohorts. Sample size calculations were based on testing the null hypothesis that sensitivity equals 0.80. In the development hospital cohort, the model demonstrated a sensitivity of 0.869 and a specificity of 0.896. With a two-sided significance level (α) of 0.05 and a power of 90%, an estimated 310 cases of LVEF ≤ 40% were required.

Given that the prevalence of left ventricular dysfunction was 4% in the development hospital cohort but expected to be lower-between 2.5% and 3%-in external validation settings (i.e., regional and local hospitals), the total sample size needed to accrue the target number of cases was estimated to range between 10,333 and 12,400 patients. To achieve this, six regional hospitals and seven local hospitals were selected as external validation sites. Because both electrocardiography and echocardiography were required within a seven-day interval-leading to anticipated exclusions-approximately 1,500 patients were targeted from each regional hospital and 500 from each local hospital, resulting in a final target sample size of approximately 12,500 patients.

02

Conditions studied

  • Cardiac Disease

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Keywords

  • left ventricular dysfunction
  • artificial intelligence
03

In context

Ventricular Dysfunction, Left Reclassified

260 studies on the registry are indexed under Ventricular Dysfunction, Left; 57 are open to participants now.

This study's planned enrollment of 12,500 is above the median of 198 across 103 observational studies indexed under Ventricular Dysfunction, Left.

Browse Ventricular Dysfunction, Left studies →

Lead sponsor

Tri-Service General Hospital is the lead sponsor of 108 studies on the registry; 11 are open to participants now.

Compared within Ventricular Dysfunction, Left, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Heart Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

All patients with ECGs and an echocardiogram within 7 days

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patients with ECGs and an echocardiogram within 7 days

Exclusion criteria

Exclusion Criteria:

  • Missing signals
  • Missing assessment in echocardiograms
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
12,500 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testAI-ECG Algorithm

    AI-ECG Algorithm to detect LVEF\<=40%

06

What researchers measure

Primary outcomes

  1. The Sensitivity and specificity of AI-ECG model for left ventricular ejection fraction ≤ 40%

    The primary objective of the study was to evaluate the sensitivity and specificity of the artificial intelligence-enabled electrocardiography (AI-ECG) model in detecting left ventricular dysfunction, defined as left ventricular ejection fraction (LVEF) ≤ 40% as confirmed by transthoracic echocardiography.

    Time frame: within 7 days

07

Study locations

13 sites
  • Hualien Armed Forces General Hospital
    Hualien City, Taiwan
  • Kaohsiung Armed Forces General Hospital Gangshan Branch
    Kaohsiung City, Taiwan
  • Kaohsiung Armed Forces General Hospital
    Kaohsiung City, Taiwan
  • Zuoying Armed Forces General Hospital
    Kaohsiung City, Taiwan
  • Tri-Service General Hospital Keelung Branch
    Keelung, Taiwan
  • Tri-Service General Hospital Penghu Branch
    Pengfu, Taiwan
  • Kaohsiung Armed Forces General Hospital Pingtung Branch
    Pingtung City, Taiwan
  • Taichung Armed Forces General Hospital Zhongqing Branch
    Taichung, Taiwan
  • Taichung Armed Forces General Hospital
    Taichung, Taiwan
  • Tri-Service General Hospital Beitou Branch
    Taipei, Taiwan
  • Tri-Service General Hospital Songshan Branch
    Taipei, Taiwan
  • Taoyuan Armed Forces General Hospital Hsinchu Branch
    Taoyuan District, Taiwan
  • Taoyuan Armed Forces General Hospital
    Taoyuan District, Taiwan
08

References and documents

Publications

  • Chen HY, Lin CS, Fang WH, Lou YS, Cheng CC, Lee CC, Lin C. Artificial Intelligence-Enabled Electrocardiography Predicts Left Ventricular Dysfunction and Future Cardiovascular Outcomes: A Retrospective Analysis. J Pers Med. 2022 Mar 13;12(3):455. doi: 10.3390/jpm12030455. PubMed 35330455 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 26, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07038018
Responsible party
Wei-Ting Liu (Clinical Doctor, Principal Investigator, Tri-Service General Hospital) — Principal investigator
First posted
Jun 26, 2025
Start date
Aug 1, 2025 (estimated)
Primary completion
Aug 31, 2025 (estimated)
Completion
Sep 30, 2025 (estimated)
Last update
Jun 26, 2025

Study contacts

Wei-Ting Liu, M.D.
Contact
wtliucv@gmail.com
+886287923311 ext. 15809

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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