Actively Recruiting

Age: 16Years +
All Genders
NCT05255705

Barts Revascularisation Registry

Led by Queen Mary University of London · Updated on 2025-07-24

20000

Participants Needed

1

Research Sites

238 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Despite the year-on-year decrease, coronary artery disease (CAD) still remains one of the leading cause of mortality worldwide. With advances in technology and our understanding of cardiac disease, we can now treat CAD using minimally invasive interventional techniques. This has revolutionised treatment for and improved the lives of many patients with CAD. Although trials have assessed various therapeutic strategies in various populations, real-world evidence of intervention and medical treatment among patients with CAD is increasingly recognised as an important part of providing safety and efficacy data and improving the care we provide. This data will add to that literature by assessing the characteristics and outcomes of patients with CAD. It will also identify and characterise predictors of outcomes, improve risk stratification and diagnostic evaluation.

CONDITIONS

Official Title

Barts Revascularisation Registry

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 16 years or older
  • Both male and female patients
  • Patients who have undergone an angiogram at Barts Heart Centre
  • Patients who have received revascularisation treatment
  • Vulnerable adults or those unable to give consent if referred to the Interventional Cardiology team
  • Patients included automatically in the database without informed consent needed
Not Eligible

You will not qualify if you...

  • Patients younger than 16 years old

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Barts Health NHS Trust

London, United Kingdom

Actively Recruiting

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Research Team

D

Dr. Krishnaraj Rathod

CONTACT

D

Dr. Daniel Jones

CONTACT

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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