Actively Recruiting

All Genders
NCT04218344

The Harefield Acute Myocardial Infarction Cohort

Led by Royal Brompton & Harefield NHS Foundation Trust · Updated on 2020-01-18

2000

Participants Needed

2

Research Sites

833 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this project the investigator's plan to collect blood during a patient's routine angiogram procedure which they will have due to having suffered a heart attack. Data from the patients' routine procedures for this condition, including but not exclusively, ECG, Echocardiogram, MRI scans, will be collected. The aim of the research project is to analyse the blood samples and identify novel biomarkers and clinical parameters associated with acute coronary syndromes. The investigator's will particularly focus on markers of inflammation and micro-organism activity. The investigator's hope that this will help to gain more knowledge about what causes heart disease and how various conditions can be treated more efficiently. The investigator's will follow-up and collect further research data via a questionnaire at the routine 6 weeks and 6 months follow-up appointment after the angiogram procedure. Participants will also be telephoned at one-year post procedure, to update any events and medication status and data will thereafter be collected form data held by the hospital without having to contact the participant. Remaining blood samples will be stored securely for further analysis into blood and other markers.

CONDITIONS

Official Title

The Harefield Acute Myocardial Infarction Cohort

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients presenting to Harefield Hospital through the Primary Percutaneous Coronary Intervention programme with ST-segment elevation myocardial infarction
  • Patients with non ST-segment elevation myocardial infarction
  • Patients with unstable angina
  • Patients with Tako Tsubo syndrome
  • Patients with spontaneous coronary artery dissection
  • Patients with acute myocarditis
  • Patients planned for coronary angiography assessment
Not Eligible

You will not qualify if you...

  • Patients who do not provide full informed consent
  • Patients who do not survive the hospital episode and for whom consent is assumed through a consultee process

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

Harefield Hospital

Harefield, Middlesex, United Kingdom, UB9 6JH

Actively Recruiting

2

Royal Brompton and Harefield NHS Foundation Trust

Uxbridge, Middlesex, United Kingdom, UB9 6JH

Actively Recruiting

Loading map...

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here