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European Quality Improvement Programme for Acute Coronary Syndromes

Improving the Management of Non-ST Elevation Acute Coronary Syndrome: Systematic Evaluation of a Quality Improvement Programme

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00716430
Acronym
EQUIP-ACS
Enrollment
3500
Registered
2008-07-16
Start date
2007-08-31
Completion date
2009-02-28
Last updated
2008-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome

Keywords

acute coronary syndromes, quality improvement

Brief summary

The main hypothesis to be tested is that the use of a quality improvement programme will lead to measurable improvements in the management of care and use of evidence based treatments for patients presenting to hospital with non-ST elevation acute coronary syndromes.

Interventions

BEHAVIORALQuality Improvement Programme

Quality Improvement training programme

Sponsors

Uppsala University
CollaboratorOTHER
GlaxoSmithKline
CollaboratorINDUSTRY
Royal Brompton & Harefield NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 80 Years
Healthy volunteers
No

Inclusion criteria

Patients with a good clinical history of ACS and at least one of the following: * New or transient ST or T wave changes on the ECG consistent with acute myocardial ischaemia * Elevation of troponin or other cardiac markers to levels indicative of myocardial necrosis according to local laboratory values

Exclusion criteria

* Evidence of persistent ST elevation on the ECG * Use of early reperfusion therapy * Patients \>80 years * Patients transferred from another hospital

Design outcomes

Primary

MeasureTime frame
Composite of 7 outcome measures to assess aggregate potential for improvement in care using the QI programme:1:risk stratification within 24 hrs, 2:early coronary angiography, 3:anticoagulation, 4:beta-blockers, 5:statins, 6:ACE-inhibitors, 7:Clopidogrel10 months

Secondary

MeasureTime frame
Estimated costs of care for patients10 months
Estimated costs and economic evaluation of potential cost-effectiveness of QI programme10 months
Clinical outcomes at discharge including death and myocardial infarction10 months

Countries

France, Italy, Poland, Spain, United Kingdom

Contacts

Primary ContactMarcus D Flather
m.flather@rbht.nhs.uk0044 (0) 207 351 8827
Backup ContactDaphne Babalis
d.babalis@rbht.nhs.uk0044 (0) 207 351 8889

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026