NCT04218344Recruiting
The Harefield Acute Myocardial Infarction Cohort
Source: ClinicalTrials.gov · Last updated 18 Jan 2020 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 2000 (estimated)
- First submitted
- 2 Jan 2020
- Start date
- 9 Jan 2020
- Primary completion date
- 31 Dec 2030
- Lead sponsor
- Royal Brompton & Harefield NHS Foundation Trust
- Diseases
- Coronary artery disease
- NCT number
- NCT04218344
What you commit to
- Study type: Observational
- Planned participants: 2000
- From 9 Jan 2020 to the primary completion date, 31 Dec 2030
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Patients will be able to self-exclude if they do not provide full informed consent
- Every effort will be made to obtain informed consent from all patients.
- Patients who do not survive the hospital episode will undergo a Professional or Personal Consultee process of assumed consent.
Who the study is looking for
- All patients presenting to Harefield Hospital through the Primary Percutaneous Coronary Intervention programme, with ST-segment elevation myocardial infarction, non ST-segment elevation myocardial infarction, unstable angina, Tako Tsubo syndrome, spontaneous coronary artery dissection and acute myocarditis, with the intention to assess with coronary angiography.
Sex: All
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Harefield Hospital Coordinator of this site? Confirm its status | Harefield | United Kingdom | Recruiting |
| Royal Brompton and Harefield NHS Foundation Trust Coordinator of this site? Confirm its status | Uxbridge | United Kingdom | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.