Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT03428048

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Valley View Hospital

Glenwood Springs, Colorado, United States, 81601

Actively Recruiting

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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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