Actively Recruiting
Cardiovascular Innovation & Research Institute 's NEXUS Registry, the Whole is Greater Than the Parts.
Led by Cardiovascular Innovation and Research Institute · Updated on 2020-06-01
1000
Participants Needed
1
Research Sites
730 weeks
Total Duration
On this page
Sponsors
C
Cardiovascular Innovation and Research Institute
Lead Sponsor
V
Valley View Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Information gathered from the patients via a disease specific questionnaire will be married to data from the National Cardiovascular Data Registry (NCDR®). Details will be continuously analyzed and used to direct quality of care at our center. The institution is categorized as a low-volume institution for percutaneous coronary intervention (PCI) for coronary artery disease treatment as well as surgical and endocardial ablation for the management of atrial fibrillation (Afib). The association between operator volume and quality has primarily focused on rare complications, such as mortality. The aim is to highlight the advantages of receiving care close to home. A benefit of offering the procedures to treat diseases at centers that have lower volumes is to improve patients' outcomes while also providing more convenient access to quality care. The key outcome from the patients' experience is alleviation of their symptoms while increasing function and quality of life. To date, there have been no studies documenting the health status benefits of PCI and surgical / endocardial ablation for coronary artery disease and Afib, respectively with low- volume operators. In this study, the investigators sought to examine the feasibility of implementing patient-reported outcomes into clinical care and to demonstrate evidence of benefits, from patients' perspectives, of receiving treatment by low-volume operators.
CONDITIONS
Official Title
Cardiovascular Innovation & Research Institute 's NEXUS Registry, the Whole is Greater Than the Parts.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Informed consent provided with understanding and agreement to study provisions
- Available for follow-up during the study
- Diagnosed with coronary artery disease or atrial fibrillation
You will not qualify if you...
- Unable or unwilling to provide informed consent
- Likely difficulties in maintaining follow-up as judged by investigators
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Valley View Hospital
Glenwood Springs, Colorado, United States, 81601
Actively Recruiting
Research Team
K
Kim M Williams, MPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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