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Coronary Artery DiseaseHEART-AINCT07837765

Heart tEam Decision-making Assisted by Revaz AI Trial

A study testing Revaz AI in people with Coronary Artery Disease, run by University of Calgary at 2 sites in Canada.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Coronary artery disease, the narrowing of the blood vessels that supply the heart, is the leading cause of death worldwide. About 2.4 million Canadian adults live with it. There are three main ways to treat it: opening the narrowed artery with a stent, heart bypass surgery, or medications alone. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Coronary Artery Disease
What is being tested?
Revaz AI
Could I receive a placebo?
No, everyone receives an active treatment
How many people
712 participants
Where
2 sitesCanada
Study dates
Apr 2027to Sep 2033
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • adult patients (≥18 years) referred for heart team discussion of coronary artery disease treatment at a participating center
  • diagnosis of obstructive coronary artery disease, defined as any stenosis ≥50% in the left main coronary artery and/or ≥70% in any other coronary artery, as confirmed by diagnostic angiography
  • any staff clinician (interventional cardiologist, cardiac surgeon, or non-invasive cardiologist) who participates in heart team discussions and contributes to coronary artery disease treatment recommendations at the participating centers

Who cannot join

  • any subsequent heart team referral for patients who are already enrolled in the trial
  • Heart Team Clinician Eligibility:
  • trainees such as fellows or residents

Trial locations and contacts

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

Canada2 sites
  • Foothills Medical Centre

    Calgary, Alberta, T2N 4Z6

    Bryan Har, 403-220-5500, bjnhar@ucalgary.ca

  • University of Ottawa Heart Institute

    Ottawa, Ontario, K1Y 4W7

    Chris Sun, 613-696-7000, chrsun@ottawaheart.ca

Other trials in Canada

About this study

Official title: HEART-AI: Heart tEam Decision-making Assisted by Revaz AI Trial

Coronary artery disease, the narrowing of the blood vessels that supply the heart, is the leading cause of death worldwide. About 2.4 million Canadian adults live with it. There are three main ways to treat it: opening the narrowed artery with a stent, heart bypass surgery, or medications alone. For many patients the best choice is clear, but for people with complicated disease or multiple health conditions, it can be genuinely difficult to know which treatment will lead to the best outcome. For these complex cases, hospitals bring together a "heart team", a group of heart specialists including cardiologists and heart surgeons, to discuss the case and recommend the best treatment. Even so, studies show that different doctors, teams, and hospitals often make different decisions for similar patients, which suggests there is room to make these decisions better.

The investigators developed a computer program called Revaz AI. It uses artificial intelligence (AI) that has learned from the health records of more than 38,000 past patients with coronary artery disease in Alberta. When given a new patient's health information, Revaz AI estimates that person's risk of dying or having a major heart problem, such as a heart attack, stroke, heart failure, or the need for another procedure, over the next 90 days to 5 years, under each of the three treatment options. In testing on past patient records, Revaz AI's predictions were more accurate than the risk scores doctors currently use. A separate study estimated that using it could improve treatment choices and reduce health care costs. However, Revaz AI has never been tested in real time with real patients.

Read more

The central question of this trial is: Do patients do better over 5 years when the heart team can see Revaz AI's risk estimates during its discussion, compared with the usual way of deciding? The investigators will also look at whether the tool changes treatment decisions, whether it makes the team more confident in its recommendations, whether patients feel better in daily life, and whether it saves the health care system money.

The study will take place at two Canadian hospitals: Foothills Medical Centre in Calgary and the University of Ottawa Heart Institute. Together, their heart teams discuss about 900 patients each year. The investigators plan to enroll 712 adult patients whose cases have been referred to the heart team. Each patient who agrees to join will be assigned by chance, like a coin flip, to one of two groups. In one group, Revaz AI's risk estimates for that patient will be shown on screen during the heart team's virtual meeting, alongside all the usual information. In the other group, the heart team will discuss the case in the usual way, without Revaz AI. Assigning patients by chance ensures the two groups are alike, so any difference in results can be traced to Revaz AI. Importantly, Revaz AI does not make decisions: in both groups, the heart team makes the recommendation, and each patient and their doctor make the final treatment choice together, just as they do now. The investigators will then follow every patient for 5 years. Most of the follow-up information - hospital stays, procedures, and major heart problems - will come from existing health databases, so patients do not need extra hospital visits. The investigators will also contact patients four times (at about 3 months, 1 year, 3 years, and 5 years) with short questionnaires about their symptoms and quality of life.

The main measure is the proportion of patients who have a major heart problem or die within 5 years of treatment. Based on past data, about 40% of similar patients experience one of these events within 5 years. The study is designed to detect whether Revaz AI can reduce this to 30%. Independent statisticians will analyze the results, and an independent safety board of experts not involved in the study will review the data regularly and can stop the study if any safety concern appears.

The study is led by university researchers with heart specialists at both hospitals. The lead researcher who co-founded the company that makes Revaz AI will stay at arm's length from the study's conduct and analysis, which will be handled by independent team members. All patient information will be coded and stored on secure hospital and university servers.

No AI tool for choosing coronary artery disease treatment has ever been tested in a rigorous trial like this. If Revaz AI improves outcomes, patients with complex heart disease could receive treatment decisions tailored to them, and the tool could be adopted by hospitals across Canada and beyond. If it does not, the study will still teach the medical community valuable lessons about how doctors and AI tools work together - knowledge that will shape the safe use of AI in health care.

Being tested
Revaz AI
Keywords
artificial intelligence, clinical decision support, coronary artery disease treatment selection
Medical subject headings
Coronary Artery Disease

What participants receive

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

  • Revaz AIBehavioural

    Revaz AI is an AI-enabled coronary artery disease treatment decision support tool that predicts short-term and long-term MACE and mortality outcomes conditioned on treatment.

Study groups in NCT07837765
Study groupRoleWhat they receive
Revaz AI-supported coronary artery disease treatment decision-makingExperimentalCoronary artery disease treatment decision-making will be supported by Revaz AI insights
Receives: Behavioral: Revaz AI
ControlNo interventionUsual coronary artery disease treatment decision-making without Revaz AI support

What is being measured

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

  1. 5-year post-treatment 5-point MACE

    5-point MACE includes myocardial infarction, heart failure, stroke, repeat revascularization, and all-cause mortality.

    Measured: 5 years post-treatment

Secondary outcomes (8)
  1. 90 days, 1 year, and 3 years post-treatment 5-point MACE

    5-point MACE includes myocardial infarction, heart failure, stroke, repeat revascularization, and all-cause mortality.

    Measured: 90 days, 1 year, and 3 years post-treatment

  2. Patient-reported Health-related Quality of Life (SAQ-7) at 90 days, 1 year, 3 years, and 5 years post-treatment

    Collected using SAQ-7

    Measured: 90 days, 1 year, 3 years, and 5 years post-treatment

  3. Patient-reported Health-related Quality of Life (EQ-5D-5L) at 90 days, 1 year, 3 years, and 5 years post-treatment

    Collected using EQ-5D-5L

    Measured: 90 days, 1 year, 3 years, and 5 years post-treatment

  4. The lead clinician's level of confidence in the heart team treatment recommendation

    Collected using the Decisional Conflict Scale

    Measured: Immediately after the heart team meeting

  5. Concordance between the heart team's final treatment recommendation and the treatment predicted by Revaz AI to yield the lowest 5-year MACE risk

    Measured: Immediately after the heart team meeting

  6. Heart team consensus

    Measured: Immediately after the heart team meeting

  7. 90-day hospital readmission

    Measured: 90 days post-treatment

  8. Total health care costs incurred during the post-treatment 5-year period

    Measured: 5 years post-treatment

Timeline

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

  1. First posted24 Sep 2026
  2. Study startApr 2027 (estimated)
  3. Primary completionSep 2033 (estimated)
  4. Study completionSep 2033 (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
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
712 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07837765
Sponsor's protocol ID
REB26-1546
Acronym
HEART-AI
Status last verified
Sep 2026
First submitted
11 Sep 2026
Last updated
24 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: There is no follow-up study planned.

Questions about this trial

What is this clinical trial studying?

A study testing Revaz AI in people with Coronary Artery Disease, run by University of Calgary at 2 sites in Canada.

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 3 inclusion and 3 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: opening soon, as of the sponsor's last update on 24 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Canada. 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?

Contact Joon Lee (403-220-2968, joon.lee@ucalgary.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

5-year post-treatment 5-point MACE (time frame: 5 years post-treatment). 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 24 Sep 2026.

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