NCT Number: NCT00716352
Prospective Registry of Outcomes and Management of Acute Ischaemic Syndromes
This is a multi-centre UK study designed to evaluate if an educational intervention programme delivered to health care professionals can improve the use of evidence based treatments in the management of patients admitted to hospital with non-ST elevation Acute Coronary Syndrome. A total of 38 centres participated, half received the educational intervention. Patients were followed to hospital discharge. Patients were followed up at 6 months. Longer term follow up through the Office Of National Statistics will be performed.
Looking for future studies?
Notify MeKey information
Conditions
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
University Hospital Aintree, Aintree, United Kingdom
About this study
This is a multi-centre UK study designed to evaluate if an educational intervention programme delivered to health care professionals can improve the use of evidence based treatments in the management of patients admitted to hospital with non-ST elevation Acute Coronary Syndrome. A total of 38 centres participated. A cluster randomised method was used and half of centres received the educational intervention. Patients were followed to hospital discharge. Patients were followed up at 6 months and longer term follow up for mortality will be performed through the national databases.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All patients admitted to the hospital (either through casualty or directly to the wards), with a good clinical history of an acute coronary syndrome with one or more of the following:
- Ischaemic changes on the admission ECG (including patients with bundle branch block)
- Elevated Troponin or cardiac enzymes on admission
- Normal ECGs but with evidence of pre-existing coronary artery disease i.e., evidence of a prior history of MI, coronary revascularisation, coronary angiography demonstrating the presence of significant coronary stenosis or a stress test demonstrating ischaemia (treadmill, echo or nuclear scan)
Written informed consent
Exclusion criteria
- Patients with persistent ST elevation >1mm in two or more contiguous leads on the ECG.
- Patients treated with thrombolytic therapy, or for whom thrombolytic therapy was considered on admission.
Treatment and study plan
Primary outcomes
-
Adherence to the educational programme measured by the frequency of use of the evidence based treatments: Aspirin, Heparin, Clopidogrel, Beta blockers, Statins.
Secondary outcomes
-
Comparison of investigations and tests
-
Use of other treatments
-
Counselling for lifestyle changes
-
Referral to smoking cessation clinics
-
Cardiac rehabilitation
-
Compliance to treatment at 6 months
-
Comparison of clinical events at 6 months
Sponsors and collaborators
Lead sponsor
Royal Brompton & Harefield NHS Foundation Trust
Other
Collaborators
- Bristol-Myers Squibb
- Sanofi
Registry information
Important dates
- Study start
- 2004
- Study completion
- 2005
- First posted
- Jul 16, 2008
- Registry last updated
- Jul 16, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Safety and Efficacy of Drug-Coated Balloon for De-novo Lesions in Patients With Acute Coronary Syndromes (DCB-ACS)
NCT04937803
ACS, Acute Coronary Syndrome
Harbin, Heilongjiang, China
View Trial DetailsPrasugrel Versus Double Dose Clopidogrel to Treat Clopidogrel Low-responsiveness After PCI
NCT01135667
Acute Coronary Syndrome, Acute Coronary Syndromes
Copenhagen O, Denmark
View Trial DetailsDiscovery of New Circulating Biomarkers of Coronary Atherosclerosis
NCT00430820
Acute Coronary Syndrome, Acute Coronary Syndromes
Paris, France
View Trial DetailsSafety and Clinical Performance of the Freesolve Resorbable Magnesium Scaffold System in the Treatment of Subjects With Long de Novo Lesions
NCT07091682
Acute Coronary Syndrome, Acute Coronary Syndromes
Erfurt, Germany
View Trial Details