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Completed

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Aintree, Aintree, United Kingdom

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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

Educational intervention programme

Behavioral

Primary outcomes

  1. Adherence to the educational programme measured by the frequency of use of the evidence based treatments: Aspirin, Heparin, Clopidogrel, Beta blockers, Statins.

Secondary outcomes

  1. Comparison of investigations and tests

  2. Use of other treatments

  3. Counselling for lifestyle changes

  4. Referral to smoking cessation clinics

  5. Cardiac rehabilitation

  6. Compliance to treatment at 6 months

  7. 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.

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