Actively Recruiting

Age: 16Years +
All Genders
ID06040528

Barts Early Post-Acute Myocardial Infarction Discharge Registry

Led by Queen Mary University of London · Updated on 2026-02-27

20000

Participants Needed

2

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Coronary artery disease (CAD) remains a leading cause of death worldwide despite improvements over time. Advances in minimally invasive treatments have improved patient outcomes, but real-world data on intervention and treatment safety and effectiveness are needed. This research focuses on patients with acute coronary syndrome discharged early after primary percutaneous coronary intervention (PCI) to better understand their characteristics and outcomes, helping improve risk assessment and care strategies. The study uses a large clinical database from a major cardiac center in Europe, including patients admitted with acute coronary syndrome and discharged early after PCI. This observational registry collects demographic, clinical, and outcome data on patients with a range of CAD complexities. The research aims to assess the safety and feasibility of the early discharge pathway and explore predictors of outcomes and complications following interventional treatment. Participants' data are collected and analyzed over one year, including medication adjustments, major adverse cardiac events, and quality of life assessments. The study uses secure databases and monitors patient outcomes to provide real-world evidence on early discharge after heart attack treatment. The findings intend to inform local and global care practices and stimulate further research in underexplored areas of cardiac care.

CONDITIONS

Brief Title

Early Discharge Pathway 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 admitted with acute coronary syndrome
  • Vulnerable adults or those unable to give consent if referred to the Interventional Cardiology team
  • Automatic inclusion in the database without need for individual consent
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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - 1 year

Participants who undergo routine care are observed after discharge via the early discharge pathway at Barts Heart Centre. Data on their health status, medication titration, and quality of life are collected.

Regular follow-up visits as per routine care

Trial Site Locations

Total: 2 locations

1

Barts Health NHS Trust

London, United Kingdom

Actively Recruiting

2

Dr. Daniel Jones

London, United Kingdom

Actively Recruiting

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Research Team

D

Dr. Daniel A Jones

D

Dr. Krishnaraj S Rathod

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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Published Research Related To This Trial

Safety and feasibility of hospital discharge 2 days following primary percutaneous intervention for ST-segment elevation myocardial infarction.

Daniel A Jones, Krishnaraj S Rathod, James Philip Howard...

https://pubmed.ncbi.nlm.nih.gov/23053711