Actively Recruiting

Age: 16Years +
All Genders
ID04440761

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

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

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.

Surveillance

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

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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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