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Not yet recruitingNCT07405866PAPPUpdated Feb 12, 2026

A Prospective Analysis To Assess The Potential Use Of ECGio In Clinical Practice

An observational study in AI-algorithm Usage, sponsored by Heart Input Output Inc. Not yet recruiting at 4 sites in United States. Open to participants aged 18 Years to 89 Years. Per ClinicalTrials.gov, last updated 2026-02-12.

Sponsored by Heart Input Output Inc · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
10,000
Ages
18 Years to 89 Years
Sex
All
01

Study summary

The goal of this observational study is to learn if an ai-assistive algorithm would be useful in patients who are under suspicion of coronary disease. The main question it aims to answer:

What proportion of patients would clinicians see fit to order an ai-assistive algorithm if available for clinical use?

Participants will be asked to use clinical judgement as to whether a patient fits a predetermined criteria for use and select them for ai-assistive analysis.

Read the detailed description

An anonymous and de-identified database to be created over the next 9 months at the Cardiology Consultants of Philadelphia. Clinicians will be given the opportunity to select patients who would be appropriate for the analysis, then the study database will be able to be collected retrospectively after the fact. The second database will be a survey response database collected anonymously and de-identified of a simple random sample of clinicians (see 6.2) who "ordered" ECGio. The EMR will be scraped by CCP after the fact to identify which patients (whether ECGio was "ordered" or not) would be appropriate for ECGio usage based on the criteria defined in section 3.1.

Digital (or PDF), anonymous, and de-identified ECG tracings for the cohort will be collected from the MUSE system. We will be provided an example of the ECG tracing as an XML export (or other format acceptable to the study sponsor), lasting 10 seconds with 500 Hz sampling. Within the digital tracing a total of 5000 data points exist for each of 12 standard leads (aVL, I, -aVR, II, aVF, III, V1, V2, V3, V4, V5, and V6).

02

Conditions studied

  • AI-algorithm Usage

Keywords

  • Artificial Intelligence
  • Advanced Usage
03

In context

Lead sponsor

Heart Input Output Inc is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 89 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

This study will be conducted in patients who fall within the guidelines for referral to calcium scoring and present at the Cardiology Consultant's of Philadelphia's Advanced Access Center, or present at one of their clinics for pre-operative screening.

Inclusion criteria

  • Age ≥ 18 years.
  • Patients with medical records stored in a digitized format.
  • Presenting between February 1 2026 and October 31 2026.
  • Patient meets one of the following criteria:

    • Hypertension
    • Hyperlipidemia
    • Family History of Disease
    • Diabetes Mellitus
    • High BMI (>30)
    • Smoker (Former or Current)
    • Presenting for pre-operative clearance

Exclusion criteria

Exclusion Criteria:

  • Patients with acute coronary syndrome (ACS).
  • Patient with prior Coronary Artery Bypass Grafting (CABG)
  • Patients whose ECG tracing has extreme noise or artifact to the extent that it would be recommended to redo the tracing.
  • Age ≥ 90 years.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
10,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • AI-Assistive Algorithm Usage

    This group is the patients who were selected as appropriate for use of the AI-Assistive algorithm.

    Device: AI-Assistive Algorithm

Interventions

  • DeviceAI-Assistive Algorithm

    ECGio is the first coronary stenosis detection software utilizing data from just a 10-second electrocardiogram (ECG). ECGs are inexpensive, non-invasive, commonly administered tests, and measure the electrical activity of the heart in "waves". The ECGio diagnostic algorithm is an ECG analytic tool which provides the clinician with information to detect the presence, severity, and location of clinically significant coronary artery disease. This diagnostic algorithm is currently not FDA approved, but once FDA approval is received, the labeling will address the following indication and use.

    Also known as: ECGio

06

What researchers measure

Primary outcomes

  1. Usage Proportion

    The proportion of patients in which it was deemed appropriate to use the AI-Assistive Algorithm

    Time frame: During or within 1 day, on average, of the patient visit

07

Study locations

4 sites
  • Cardiology Consultants of Philadelphia - Rothman Orthopedics
    Bensalem, Pennsylvania 19020, United States
  • Cardiology Consultants of Philadelphia - Chestnus St
    Philadelphia, Pennsylvania 19107, United States
  • Cardiology Consultants of Philadelphia
    Philadelphia, Pennsylvania 19148, United States
  • Cardiology Consultants of Philadelphia - Sproul
    Springfield, Pennsylvania 19064, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07405866
Lead sponsor
Heart Input Output Inc
Responsible party
Sponsor
First posted
Feb 12, 2026
Start date
Feb 21, 2026 (estimated)
Primary completion
Nov 21, 2026 (estimated)
Completion
Nov 21, 2026 (estimated)
Last update
Feb 12, 2026

Study contacts

Michael Leasure
Contact
Michael.Leasure@heartio.ai
6104517343
Veronica Covalesky, MD
principal investigator · Cardiology Consultants of Philadelphia

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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