GenesisCare Cardiovascular Outcomes Registry of Australian Percutaneous Coronary Intervention and Cardiac Implantable Electronic Device Patients
A clinical prospective registry of Percutaneous Coronary Intervention and Cardiac Implantable Electronic Device patients treated at GenesisCare affiliated hospitals in Australia (A168/08)
GenesisCare Cardiology
50,000 participants
Dec 2, 2008
Observational
Conditions
Summary
The GenesisCare Outcomes Registry (GCOR) was established in November 2008 and is designed to improve patient care and outcomes through greater understanding of events, treatment and outcomes. The Registry collects detailed clinical, procedural and outcomes data on GenesisCare patients undergoing Percutaneous Coronary Intervention (PCI) or Cardiac Implantable Electronic Device (CIED) implantations. In order to improve the quality care and guideline compliance in Australia with National Outcome Registries, the registry aims to capture 100% of GenesisCare patients to monitor and benchmark compliance, care and outcomes, provide a national set of risk adjusted, consumer-focused and current clinical performance indicators to reflect clinical variations and patient outcomes. The registry will also inform research and the scientific community on coronary disease through publications/presentations, support evidence-based therapies, create efficiencies in healthcare and contribute to reducing mortality and morbidity.
Eligibility
Plain Language Summary
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Interventions
The GenesisCare Cardiovascular Outcomes Registry (GCOR) is a clinical quality register established to collect information on all patients undergoing Percutaneous Coronary Intervention (PCI) or Cardiac Implantable Electronic Device (CIED) implantation at GenesisCare affiliated hospital sites across Australia. Clinical Research Assistants from GenesisCare will collect information pertaining to the participants medical history, demographic and procedural data, medication use, and follow-up cardiac health outcomes utilising data-linkage to medical records and from participants by phone. Clinical Research Assistants will contact participants by phone at 30 days, 1, 2, 3, 4, 5 and 10 years post-procedure, to briefly obtain information about their heart health. Participants will be asked about any new cardiac symptoms, EQ-5D-5L Quality of Life questionnaire, any further procedural and/or hospital admissions that may have occurred and medication use. Performance and outcome measure feedback will be provided to participating hospitals and health care providers to allow benchmarking against national and international results, although this data will be de-identified in reports.
Locations(11)
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ACTRN12620000899943