GenesisCare Cardiovascular Outcomes Registry of Australian Percutaneous Coronary Intervention and Cardiac Implantable Electronic Device Patients

Not Applicable

Recruiting

• Conditions: Coronary Artery Disease; Percutaneous Coronary Intervention; Heart Failure; Permanent Pacemaker; Implantable Cardioverter Defibrillator; Cardiac Arrhythmia; Cardiovascular - Coronary heart disease; Cardiovascular - Other cardiovascular diseases

• Registration Number: ACTRN12620000899943
• Lead Sponsor: GenesisCare Cardiology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-09-11
• Last Update Posted: 21 September 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50000

Inclusion Criteria

This registry will include all patients from GenesisCare Cardiology practices who are undergoing Percutaneous Coronary Intervention (PCI) or Cardiac Implantable Electronic Device (CIED) implantation at a GenesisCare Cardiology affiliated hospital.

Exclusion Criteria

exclusion criteria.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary purpose of this registry is to improve patient care by evaluating care delivered through PCI and CIED implantations and provide significant real-world data on patients, procedures, treatments and outcomes to health care providers. For example, the following outcome measures are collated;<br><br>Assessment of post-procedure complications, including hospital readmission rates, will be determined by follow-up telephone survey and data-linkage to medical records.<br><br><br><br>[During hospital admission for clinically indicated procedure, and 30 days, 1, 2, 3, 4, 5 and 10 years post-procedure.];Health outcomes (e.g. complications – haemorrhage, stroke, myocardial infarction, mortality) will be determined by follow-up telephone survey and data-linkage to medical records.[During hospital admission for clinically indicated procedure, and 30 days, 1, 2, 3, 4, 5 and 10 years post-procedure.]

Secondary Outcome Measures

Name	Time	Method
Patient Reported Outcome Measures e.g. change in health-related quality of life will be assessed using the EQ-5D-5L questionnaire, <br><br>[During hospital admission for clinically indicated procedure and 1 year post-procedure.]