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.
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
- Type of treatment
- Lifestyle or therapy programme
- 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
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.
- Conditions
- Coronary Artery Disease
- 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 group | Role | What they receive |
|---|---|---|
| Revaz AI-supported coronary artery disease treatment decision-making | Experimental | Coronary artery disease treatment decision-making will be supported by Revaz AI insights Receives: Behavioral: Revaz AI |
| Control | No intervention | Usual 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.
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)
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
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
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
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
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
Heart team consensus
Measured: Immediately after the heart team meeting
90-day hospital readmission
Measured: 90 days post-treatment
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.
- First posted24 Sep 2026
- Study startApr 2027 (estimated)
- Primary completionSep 2033 (estimated)
- Study completionSep 2033 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Coronary Artery DiseaseStudies of the same condition, open and under way.
- More trials run by University of CalgaryThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Calgary
- Sponsor type
- University, hospital or other
- Collaborators
- University of Ottawa Heart Institute, Canada, Foothills Medical Centre, Alberta Health services
- Responsible party
- Sponsor
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.
Study at a glance
From the registry record, last updated by the sponsor on 24 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- HEART-AI: Heart tEam Decision-making Assisted by Revaz AI Trial
- ClinicalTrials.gov ID
- NCT07837765
- Acronym / sponsor ID
- HEART-AI / REB26-1546
- Conditions
- Coronary Artery Disease
- Keywords
- artificial intelligence, clinical decision support, coronary artery disease treatment selection
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 712 participants (estimated)
- Lead sponsor
- University of CalgaryUniversity, hospital or other
- Collaborators
- University of Ottawa Heart Institute, Canada, Foothills Medical Centre, Alberta Health services
- Study start
- Apr 2027 (estimated)
- Primary completion
- Sep 2033 (estimated)
- Study completion
- Sep 2033 (estimated)
- First posted
- 24 Sep 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Revaz AI-supported coronary artery disease treatment decision-making | Experimental | Behavioral: Revaz AICoronary artery disease treatment decision-making will be supported by Revaz AI insights |
| Control | No intervention | –Usual coronary artery disease treatment decision-making without Revaz AI support |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (3 listed)
- Heart Team Clinician Eligibility:
- trainees such as fellows or residents
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Revaz AIRevaz 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. | Behavioural | Revaz AI-supported coronary artery disease treatment decision-making |
Primary outcome
5-year post-treatment 5-point MACE
Time frame: 5 years post-treatment
5-point MACE includes myocardial infarction, heart failure, stroke, repeat revascularization, and all-cause mortality.
8 secondary outcomes
90 days, 1 year, and 3 years post-treatment 5-point MACE
Time frame: 90 days, 1 year, and 3 years post-treatment
Patient-reported Health-related Quality of Life (SAQ-7) at 90 days, 1 year, 3 years, and 5 years post-treatment
Time frame: 90 days, 1 year, 3 years, and 5 years post-treatment
Patient-reported Health-related Quality of Life (EQ-5D-5L) at 90 days, 1 year, 3 years, and 5 years post-treatment
Time frame: 90 days, 1 year, 3 years, and 5 years post-treatment
The lead clinician's level of confidence in the heart team treatment recommendation
Time frame: Immediately after the heart team meeting
Concordance between the heart team's final treatment recommendation and the treatment predicted by Revaz AI to yield the lowest 5-year MACE risk
Time frame: Immediately after the heart team meeting
Heart team consensus
Time frame: Immediately after the heart team meeting
90-day hospital readmission
Time frame: 90 days post-treatment
Total health care costs incurred during the post-treatment 5-year period
Time frame: 5 years post-treatment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Sep 2026.
- Individual participant dataSharing planned: No. There is no follow-up study planned.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
2 sites in 1 country: see every site and its status.
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.