Stratified medicine approach for managing angina without obstructive coronary artery disease
International Study of Coronary Microvascular Angina (iCorMicA): a Randomised, Controlled, Multicentre Trial and Registry
This study is testing if a personalized treatment plan based on a special heart test can help people with angina who don’t have blocked arteries feel better and improve their health.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 1500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | NHS Greater Glasgow and Clyde Academic / other |
| Locations | 39 sites (Cork and 38 other locations) |
| Trial ID | NCT04674449 on ClinicalTrials.gov |
What this trial studies
The iCorMicA study is a multicentre, prospective, randomised, double-blind, sham-controlled trial aimed at improving the management of patients with angina who do not have obstructive coronary artery disease. It evaluates whether tailored medical therapy, guided by an interventional diagnostic procedure during invasive coronary angiography, can enhance patient symptoms, wellbeing, and clinical outcomes. The study builds on previous findings that suggest stratified medicine may significantly benefit patients with microvascular angina and related conditions. Participants will be randomly assigned to receive either the results of the diagnostic procedure or a sham intervention.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for invasive coronary angiography and exhibit symptoms of angina.
Not a fit: Patients with obstructive coronary artery disease or those undergoing angiography for non-coronary reasons may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved symptom management and quality of life for patients with microvascular angina.
How similar studies have performed: Previous studies, such as the CorMicA pilot, have shown promising results for similar stratified medicine approaches in managing ischaemic heart disease.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age ≥18 years. 2. A clinical plan for invasive coronary angiography. 3. Symptoms of angina (typical or atypical) according to the Rose- and/or Seattle Angina questionnaires. 4. Able to comply with study procedures. 5. Able to provide informed consent. Exclusion Criteria: 1. A non-coronary primary indication for invasive angiography (e.g. valve disease, heart failure). 2. History of coronary artery bypass surgery. 3. Presence of obstructive disease evident in a main coronary artery (diameter \>2.5 mm), i.e. a coronary stenosis \>50% and/or a fractional flow reserve (FFR) ≤0.80\*. 4. Logistical reason\*. \*These patients will enter a follow-up registry.
Where this trial is running
Cork and 38 other locations
- Mater Private Hsopital — Cork, Ireland (Completed)
- Mater Private Hospital — Dublin, Ireland (Completed)
- Radboud University Medical Centre — Nijmegen, Netherlands (Recruiting)
- 5th Military Hospital — Krakow, Poland (Recruiting)
- Golden Jubilee National Hospital — Clydebank, Scotland, United Kingdom (Recruiting)
- Aberdeen Royal Hospital — Aberdeen, United Kingdom (Completed)
- William Harvey Hospital — Ashford, United Kingdom (Recruiting)
- Basildon University Hospital - Essex Cardiothoracic Centre — Basildon, United Kingdom (Completed)
- Bedford Hospital NHS Trust — Bedford, United Kingdom (Recruiting)
- Royal Victoria Hospital — Belfast, United Kingdom (Recruiting)
- Birmingham Heartlands Hospital — Birmingham, United Kingdom (Recruiting)
- Royal Blackburn Teaching Hospital — Blackburn, United Kingdom (Recruiting)
- Victoria Hospital — Blackpool, United Kingdom (Recruiting)
- Glan Clwyd Hospital — Bodelwyddan, United Kingdom (Recruiting)
- Royal Bournemouth Hospital — Bournemouth, United Kingdom (Completed)
- Royal Papworth Hospital NHS Foundation Trust — Cambridge, United Kingdom (Active_not_recruiting)
- University Hospital of Wales — Cardiff, United Kingdom (Recruiting)
- St Peter's Hospital NHS Foundation Trust — Chertsey, United Kingdom (Recruiting)
- University Hospitals Coventry & Warwickshire NHS Trust — Coventry, United Kingdom (Recruiting)
- University Hospital Hairmyres — East Kilbride, United Kingdom (Recruiting)
- NHS Greater Glasgow and Clyde — Glasgow, United Kingdom (Not_yet_recruiting)
- Raigmore Hospital — Inverness, United Kingdom (Recruiting)
- Leeds Teaching Hospital NHS Trust — Leeds, United Kingdom (Recruiting)
- Liverpool Heart and Chest Hospital — Liverpool, United Kingdom (Recruiting)
- Royal Free Hospital — London, United Kingdom (Recruiting)
- Barts Health NHS Trust - St. Bartholomew's Hospital — London, United Kingdom (Active_not_recruiting)
- King's College Hospital — London, United Kingdom (Recruiting)
- Northwick Park Hospital — London, United Kingdom (Recruiting)
- The Newcastle upon Tyne Hospitals NHS Foundation Trust — Newcastle upon Tyne, United Kingdom (Recruiting)
- Royal Gwent Hospital — Newport, United Kingdom (Recruiting)
- Nottingham University Hospitals NHS TRUST — Nottingham, United Kingdom (Recruiting)
- Queen Alexandra Hospital — Portsmouth, United Kingdom (Recruiting)
- Northern General Hospital — Sheffield, United Kingdom (Recruiting)
- University Hospital Southampton — Southampton, United Kingdom (Recruiting)
- South Tyneside and Sunderland NHS Foundation Trust — Sunderland, United Kingdom (Recruiting)
- Morriston Hospital — Swansea, United Kingdom (Recruiting)
- Pinderfields General Hospital — Wakefield, United Kingdom (Recruiting)
- Watford general Hospital — Watford, United Kingdom (Completed)
- New Cross Hospital — Wolverhampton, United Kingdom (Recruiting)
Study contacts
- Study coordinator: Colin Berry, MBChB, PhD
- Email: colin.berry@glasgow.ac.uk
- Phone: +44 141 330 3325
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.