Actively Recruiting
Barts Myocardial Infarction With Non-Obstructed Coronary Arteries (MINOCA) Registry
Led by Queen Mary University of London · Updated on 2025-11-18
3000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients diagnosed with myocardial infarction with non-obstructive coronary arteries (MINOCA), a condition affecting 1 to 13% of those with acute myocardial infarction. This condition presents challenges because coronary revascularization is not suitable, and current guidelines for management are lacking. The study aims to better understand the diagnosis, treatment, and long-term outcomes for these patients, whose prognosis is uncertain but guarded compared to those with obstructive coronary artery disease. This observational study uses a clinical database collecting information on all patients referred to the Interventional Cardiology team at Barts Health NHS Trust since April 2015. It includes patients aged 16 years and older with MINOCA or unclear causes of troponin rise. No additional procedures or investigations are performed solely for research. Both medically managed patients and those undergoing interventions are included, and data are anonymized before analysis. Participants' clinical data are collected during routine care without extra visits or procedures. Researchers assess outcomes such as mortality at 30 days and 1 year, formal diagnosis timing and cause of troponin rise, and changes in symptoms two months after initial review. The study continues indefinitely, aiming to evaluate the safety, feasibility, and effectiveness of further investigations in patients with MINOCA in a real-world setting.
CONDITIONS
Brief Title
Barts-MINOCA Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Both male and female patients 16 years of age or older
- Patients diagnosed with MINOCA
- Patients with no clear cause of troponin rise
You will not qualify if you...
- Patients younger than 16 years of age
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Participants are identified through routine clinical care without additional visits for research purposes.
Duration - Indefinite
Participants who undergo routine care are observed. Clinical data is collected from hospital records without additional procedures for research.
Data is collected during regular clinical visits as part of routine care.
Trial Site Locations
Total: 1 location
1
Barts Health NHS Trust
London, United Kingdom
Actively Recruiting
Research Team
D
Daniel Jones, MBBS, PhD
K
Krishnaraj Rathod, MBBS, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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