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Can a 10-Second chest scan reveal hidden heart clues?

NCT ID NCT07805213

Diagnosis Sponsor: KardioVis S.r.l. Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 04, 2026 · Last updated Sep 04, 2026

Summary

Researchers are testing a new device called KV-PREDICT that sits on the chest, over clothing, and records heart signals for about 10 seconds. The study includes 120 adults with heart failure across different severity levels. The goal is to see if the device can capture clear, repeatable signals that could later help doctors assess heart function. This pilot study does not guide treatment decisions and offers no direct benefit to participants.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
KV-PREDICT, a non-invasive chest device that records heart signals
What this could lead to
If the device reliably captures heart signals, it could become a simple, clothing-friendly way to monitor heart function in heart failure patients.
What could go wrong
This is an early pilot study focused on signal quality, not on diagnosing or predicting outcomes. The device may not perform consistently across different patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 120 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18 years or older * Clinical diagnosis of heart failure * NYHA functional class I, II, or III * Able to understand the study information and provide written informed consent * Attending a scheduled outpatient follow-up visit at the site Exclusion Criteria: * Acute clinical instability at the time of the visit * Conditions that, in the investigator's judgment, could interfere with correct performance of the acquisition procedure * Inability to provide valid informed consent * Concurrent participation in other studies that could interfere with the aims of this investigation

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Conditions

The condition(s) this trial relates to.

heart failure

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Heart failure

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • S.C. Cardiologia, Azienda Ospedaliero-Universitaria Policlinico di Modena

    Modena, Emilia-Romagna, 41124, Italy

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