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Active, not recruitingNCT05781087OCT-RISKUpdated Jun 16, 2026

Predicting the Risk of Non-culprit Coronary Artery Disease After a Heart Attack

An observational study in Coronary Artery Disease, ST Elevation Myocardial Infarction and Ischemic Heart Disease, sponsored by Guy's and St Thomas' NHS Foundation Trust. Active, not recruiting at 3 sites in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-16.

Sponsored by Guy's and St Thomas' NHS Foundation Trust · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
90
Ages
18 Years and older
Sex
All
01

Study summary

Heart attacks caused by the complete blockage of a heart artery are treated by opening it with a stent. However, most people will also have 'non-culprit' narrowings found in their other arteries at this time.

Although in general people do better if these non-culprit narrowings are also treated with stents if they look severe, this process has problems. This is because narrowings that look severe may be stable and not cause any trouble. For these people a stent is a wasted procedure and unnecessary risk. On the other hand, narrowings that are currently left alone because they appear mild, may progress and cause a heart attack.

Participants who have had a heart attack will have a scan from inside the heart arteries during an angiogram (optical coherence tomography, OCT) and a magnetic resonance angiogram (MRA).

If the investigators can show that it is possible to accurately predict which non-culprit narrowings are going to progress and which are going to stabilise, medical professionals may be able to better target their treatments after a heart attack.

02

Conditions studied

  • Coronary Artery Disease
  • ST Elevation Myocardial Infarction
  • Ischemic Heart Disease

Keywords

  • optical coherence tomography
  • non-culprit
  • magnetic resonance imaging
  • cardiac magnetic resonance
  • STEMI
  • magnetic resonance angiography
  • OCT
03

In context

Coronary Artery Disease

5,598 studies on the registry are indexed under Coronary Artery Disease; 957 are open to participants now.

This study's enrollment of 90 is below the median of 336 across 1,947 observational studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

Guy's and St Thomas' NHS Foundation Trust is the lead sponsor of 284 studies on the registry; 79 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients after presentation with ST elevation myocardial infarction.

Inclusion criteria

  • Successful primary percutaneous coronary intervention (PCI) within the previous week with no major complications at the index procedure
  • Bystander disease in a non-culprit vessel planned for clinically indicated staged angiography +/- PCI
  • Able to provide written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Cardiogenic shock requiring intubation, inotropes or a mechanical support device
  • Creatinine clearance \<30ml/min
  • Prior coronary artery bypass grafting
  • Life expectancy less than 3 years
  • Pregnancy.
  • Target lesion in the left main coronary artery
  • Severe calcification or tortuosity that would threaten safe placement of a pressure wire or OCT catheter
  • Chronic total occlusion of a major epicardial vessel.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
90 participants (actual)
Patient registry
No

Groups and cohorts

  • Standard of care

    Patients after ST-elevation myocardial infarction with non-culprit coronary artery disease.

    Diagnostic Test: Optical coherence tomography and pressure wire assessment · Diagnostic Test: Cardiac magnetic resonance angiogram

Interventions

  • Diagnostic testOptical coherence tomography and pressure wire assessment

    Non-culprit coronary arteries

    Also known as: OCT (Abbott), PressureWire X (Abbott)

  • Diagnostic testCardiac magnetic resonance angiogram

    1.5T

    Also known as: Cardiac MRI

06

What researchers measure

Primary outcomes

  1. Change in mean fibrous cap thickness measured by optical coherence tomography

    Time frame: 6 months

Secondary outcomes

  1. Change in mean lipid arc measured by optical coherence tomography

    Time frame: 6 months

  2. Presence of thin cap fibroatheroma measured by optical coherence tomography

    Plaque with lipid arc \>90° and fibrous cap thickness ≤65µm

    Time frame: 6 months

  3. Change in measures of shear stress made by optical coherence tomography and magnetic resonance angiography

    Comparison between non-invasive and invasively derived measures

    Time frame: 0 and 6 months

Other outcomes

  1. Non-culprit major adverse cardiac events

    Death, myocardial infarction, ischaemia driven revascularisation

    Time frame: 6 months and 36 months

  2. Change in vessel stenosis measured by optical coherence tomography and magnetic resonance angiography

    Comparison between non-invasive and invasively derived measures

    Time frame: 0, 6 and 36 months

07

Study locations

3 sites
  • Royal Bournemouth Hospital
    Bournemouth, United Kingdom
  • St Thomas' Hospital
    London, SE1 7EH, United Kingdom
  • King's College Hospital
    London, SE5 9RS, United Kingdom
08

References and documents

Individual participant data

Plan to share: No

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 Jun 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05781087
Lead sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborators
King's College London, Imperial College London
Responsible party
Sponsor
First posted
Mar 23, 2023
Start date
Apr 25, 2023
Primary completion
Jul 1, 2026 (estimated)
Completion
Sep 1, 2028 (estimated)
Last update
Jun 16, 2026

Study contacts

Divaka Perera, MD
principal investigator · King's College London

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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