Actively Recruiting
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
Eligibility Criteria
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
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
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
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
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