Understanding heart artery disease using biomarkers and imaging in Oxford
Official title: Multimodal Biomarkers in Coronary Artery Disease Pathogenesis: The Oxford Acute Myocardial Infarction Study (OXAMI Study)
Run by University of Oxford · NCT07772570 · Data updated 2026-11-12
Researchers in Oxford are testing how biomarkers and advanced imaging can help explain why some heart artery plaques are unstable and how this affects heart damage after a heart attack.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 90 Years |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | University of Oxford Academic / other |
| Locations | 1 site (Oxford) |
| Status | Recruiting |
| Started | May 2012 |
| Main results expected | September 2046 |
| Study ends | December 2046 |
| Registry record updated | August 24, 2026 |
| Trial ID | NCT07772570 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with evidence of myocardial injury or those scheduled for coronary angiography with PCI, in either non-emergency or emergency settings, who can safely undergo the required imaging procedures.
✕Probably not a fit
Patients with severe safety concerns, anaemia (Hb <9 g/dL), pregnancy, or contraindications to MRI or iodinated/gadolinium contrast are less likely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study combines blood tests with multiple imaging methods to explore the biology and imaging features of coronary artery disease and myocardial injury. It looks at upstream plaque behavior in the arteries and how it translates to heart muscle damage using intracoronary imaging, MRI, CT, and invasive physiology. Participants are adults with evidence of myocardial injury or those planned for coronary angiography with PCI, under non-emergency or emergency settings. The study seeks to identify multimodal biomarkers and imaging signals associated with disease progression and injury patterns. Lead sponsorship is from the University of Oxford and the Oxford Heart Centre at John Radcliffe Hospital.
Why it matters
Potential benefit: Findings could improve risk stratification and personalize how doctors monitor and treat myocardial injury and coronary artery disease.
How similar studies have gone: Previous programs in coronary artery disease have demonstrated value from multimodal imaging, though this specific combined approach is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Patients in whom safety or clinical concerns preclude participation. * Anaemia (Hb \<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 * eGFR\< 30 ml/min (stage 3-5 renal disease)
Where it's running
-
Oxford Heart Centre, John Radcliffe Hospital
Oxford, United Kingdom Recruiting
Study contacts
- Principal investigator: Keith M Channon — University of Oxford
- Study coordinator: Keith M Channon, MD
- Email: keith.channon@cardiov.ox.ac.uk
- Phone: +44 1865 287581
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.