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RecruitingNCT07772570OXAMIUpdated Aug 24, 2026

Multimodal Biomarkers in Coronary Artery Disease Pathogenesis: The Oxford Acute Myocardial Infarction Study (OXAMI Study)

An observational study in Myocardial Injury, Atherosclerosis Cardiovascular Disease and Cardiac Imaging Techniques, sponsored by University of Oxford. Recruiting at 1 site in United Kingdom. Open to participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-24.

Sponsored by University of Oxford · Observational

From the registry’s dates

  • Started May 2012; still recruiting 14 years 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,000
Ages
18 Years to 90 Years
Sex
All
01

Study summary

Coronary artery disease is one of the most common causes of illness and death. It develops when fatty deposits, known as plaques, build up in the arteries that supply blood to the heart. These plaques can gradually narrow the arteries and reduce blood flow, causing symptoms such as chest pain (angina). Sometimes a plaque can suddenly break open, causing a blood clot to form and block the artery. This can lead to a heart attack and permanent damage to the heart muscle.

Although much has been learned about coronary artery disease, important questions remain about why some plaques suddenly become unstable, how this affects blood flow through the smallest blood vessels of the heart, and why some patients develop more heart muscle damage than others.

The Oxford Acute Myocardial Infarction (OxAMI) research programme aims to improve our understanding of these processes. The investigators will study both the disease within the coronary arteries (the "upstream" problem) and its effects on the heart muscle (the "downstream" damage). By examining these together, the investigators hope to understand more clearly how changes in coronary plaques lead to heart injury and how this differs between patients.

Participants undergoing procedures to investigate or treat coronary artery disease provide an important opportunity to study these processes. During coronary angioplasty (also called percutaneous coronary intervention or PCI), a narrow or blocked artery is opened, usually using a small balloon and a stent. This procedure can disturb the underlying plaque in a similar way to the plaque disruption that occurs during a heart attack. Where appropriate, the investigators may therefore collect blood and material released from the plaque during these procedures. Blood may be collected from different locations in the circulation, allowing the investigators to study substances released by the plaque and heart muscle. Material that would otherwise be discarded during treatment may also be collected for laboratory analysis.

The investigators will use several established and newer techniques to examine the coronary arteries, the small blood vessels within the heart, and the heart muscle. These may include detailed imaging from inside the coronary arteries using intravascular ultrasound (IVUS) or optical coherence tomography (OCT). The investigators may also measure blood pressure and flow within the coronary arteries to assess how well the small blood vessels supplying the heart are working.

Non-invasive heart scans may include cardiovascular magnetic resonance (CMR/MRI), cardiac computed tomography (CT) and echocardiography (ultrasound). These techniques can provide detailed information about the structure and function of the heart, blood supply to the heart muscle, areas of injury or permanent scarring, and changes that occur following a heart attack. In particular, MRI may help distinguish heart muscle that has been permanently damaged from muscle that is injured but could potentially recover after blood flow is restored. This may be especially important for participants who arrive at hospital several hours after their heart attack began.

Other measurements may include electrocardiograms (ECGs), which record the electrical activity of the heart, and measurements of heart pressure, volume and function. Some participants may also have longer-term ECG monitoring.

Blood and tissue samples may be analysed using a range of laboratory techniques. These studies will investigate inflammation, blood clotting and other biological processes involved in coronary artery disease and heart attacks. Newer laboratory methods may allow us to measure large numbers of proteins and small molecules in the blood. Material collected from plaques may also be examined under a microscope to identify its cells and structural components.

With additional consent, blood samples may be stored for genetic research. This could help us understand whether differences in people's genes influence their risk of coronary artery disease, their response to a heart attack, or the amount of heart damage that occurs.

By combining information about coronary plaques, blood flow through the heart's circulation, heart muscle injury, imaging, blood and tissue markers, and genetic factors, the OxAMI study aims to build a detailed picture of coronary artery disease and heart attacks. The programme will establish a carefully characterised group of research participants who may contribute to future OxAMI studies conducted under separate research protocols.

Ultimately, this research aims to identify better ways to predict, diagnose and understand coronary artery disease and heart attacks, and to identify new approaches that could improve treatment and outcomes for future patients.

02

Conditions studied

  • Myocardial Injury
  • Atherosclerosis Cardiovascular Disease
  • Cardiac Imaging Techniques
  • Genetics
  • Thrombus
  • Trained Immunity
  • Biomarker Discovery
  • Coronary Physiology
  • Intravascular Imaging and Microvascular Obstruction

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03

In context

Thrombosis

955 studies on the registry are indexed under Thrombosis; 171 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 173 across 384 observational studies indexed under Thrombosis.

Browse Thrombosis studies →

Lead sponsor

University of Oxford is the lead sponsor of 812 studies on the registry; 119 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Patients presenting with evidence of myocardial injury (e.g. elevation of troponin or other cardiac biomarkers, ECG changes, wall motion abnormalities on cardiac imaging) AND/OR referred for coronary angiography with view to proceed to PCI as indicated in either non-emergency or emergency settings.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Evidence of myocardial injury (e.g. elevation of troponin or other cardiac biomarkers, changes, wall motion abnormalities on cardiac imaging) AND/OR referred for coronary angiography with view to proceed to PCI as indicated in either non-emergency or emergency settings.

Exclusion criteria

Exclusion Criteria:

  • Patients in whom safety or clinical concerns preclude participation.
  • Anaemia ( \<9).
  • Pregnant or breast feeding females.

Additional exclusion criteria for patients undergoing MRI

  • claustrophobia which limits / prevents participants from remaining in MRI scanner.
  • patients who cannot lie flat on the scan table.
  • patients with metallic implants, pacemakers, implantable defibrillators etc, unless known to be MRI compatible.
  • patients with known allergy to medium of contrast (gadolinium)

Additional exclusion criteria for patients undergoing coronary CT angiography

  • patients with a known allergy to iodinated contrast media
  • \< 30 ml/min (stage 3-5 renal disease)
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,000 participants (estimated)
Target follow-up
20 Years
Patient registry
Yes

Groups and cohorts

  • Acute Coronary Syndrome

    Patients presenting with Acute Coronary syndrome (ST-segment elevation or non-ST-Segment Elevation

    Diagnostic Test: blood sampling · Diagnostic Test: Intracoronary Imaging · Diagnostic Test: Cardiovascular Magnetic Resonance Imaging · Diagnostic Test: Cardiac Computerised Tomography · Diagnostic Test: Invasive Coronary Physiology

  • Stable ischemic heart disease

    Patients presenting with suspicion of stable ischemic heart disease

    Diagnostic Test: blood sampling · Diagnostic Test: Intracoronary Imaging · Diagnostic Test: Cardiovascular Magnetic Resonance Imaging · Diagnostic Test: Cardiac Computerised Tomography · Diagnostic Test: Invasive Coronary Physiology

  • Myocardial Injury

    Patients presenting with objective evidence of myocardial injury

    Diagnostic Test: blood sampling · Diagnostic Test: Intracoronary Imaging · Diagnostic Test: Cardiovascular Magnetic Resonance Imaging · Diagnostic Test: Cardiac Computerised Tomography · Diagnostic Test: Invasive Coronary Physiology

  • Healthy Controls

    Healthy controls

    Diagnostic Test: blood sampling · Diagnostic Test: Cardiovascular Magnetic Resonance Imaging

Interventions

  • Diagnostic testblood sampling

    Blood sampling across different periprocedural and follow-up timepoints.

  • Diagnostic testIntracoronary Imaging

    Intracoronary Imaging with approved devices

  • Diagnostic testCardiovascular Magnetic Resonance Imaging

    Cardiovascular Magnetic Resonance Imaging (Multiparametric Phenotyping)

  • Diagnostic testCardiac Computerised Tomography

    Photon-counting CT

  • Diagnostic testInvasive Coronary Physiology

    Angiography derived, Bolus Thermodilution, Continuous Thermodilution, Doppler Flow

06

What researchers measure

Primary outcomes

  1. Major adverse cardiovascular events

    Composite of cardiac mortality, heart failure, recurrent myocardial infarction, target vessel/lesion revascularization, life threatening arrhythmia

    Time frame: 20 years

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Data may be shared upon reasonable request

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 Aug 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07772570
Responsible party
Sponsor
First posted
Aug 19, 2026
Start date
May 2012
Primary completion
Sep 2046 (estimated)
Completion
Dec 2046 (estimated)
Last update
Aug 24, 2026

Study contacts

Keith M Channon, MD
Contact
keith.channon@cardiov.ox.ac.uk
+44 1865 287581
Keith M Channon
principal investigator · University of Oxford

Oversight

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

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