AI may spot deadly heart rhythms before they strike
NCT ID NCT07792694
First seen Aug 28, 2026 · Last updated Aug 28, 2026
Summary
This study tests whether artificial intelligence can use continuous ECG data to predict and detect life-threatening heart arrhythmias in patients admitted with acute cardiac illness. Researchers will analyze stored ECG data from 3000 adult patients to see if AI models can forecast ventricular tachycardia or fibrillation up to 30 minutes and 1 day ahead. The goal is to improve timely intervention and reduce false alarms that contribute to alarm fatigue.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Artificial intelligence models analyzing continuous ECG data
- What this could lead to
- If successful, this could lead to AI tools that help doctors predict and detect dangerous heart rhythms earlier, potentially reducing alarm fatigue and improving patient safety.
- What could go wrong
- This is an observational study, so it won't directly test a treatment. The AI models may not perform well enough in real-world settings, and the results may not apply to all hospitals.
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.
- Participants
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About 3,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2023
- Expected to finish
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Apr 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients aged 18 years or older admitted to the Catharina hospital Eindhoven (CZE) with cardiac diseases from 1/1/2023.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Patients admitted from 1/1/2023\* * Patients aged 18 years or older * Admitted for acute cardiac illness or after elective cardiac procedures * Who are on ECG monitoring in the CCU, ICU or ward * Patients for whom continuous waveform ECG data have been routinely stored. * Continuous waveform ECG data has been routinely stored in the CZE since 1/1/2023 on the ICU, since 1/12/2025 on the CCU and on the ward it has yet to be implemented. As our project utilizes this continuous ECG data, it will only include patients for whom this data is available. Exclusion Criteria: \- Patients who expressed their preference for not having their data used for scientific research or to improve quality of care in the opt-out program of the CZE.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Catharina Hospital Eindhoven
RECRUITINGEindhoven, North Brabant, 5623 EJ, Netherlands
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