NCT03428048Recruiting
Cardiovascular Innovation & Research Institute 's NEXUS Registry, the Whole is Greater Than the Parts.
NEXUS Registry: An Outcomes Database Which Tracks Patient -Reported Outcomes After Percutaneous Coronary Intervention for Coronary Artery Disease Along With Surgical and Subcutaneous Ablation for the Management of Atrial Fibrillation.
Source: ClinicalTrials.gov · Last updated 1 Jun 2020 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 1000 (estimated)
- First submitted
- 15 Mar 2016
- Start date
- 1 Mar 2016
- Primary completion date
- 31 Mar 2026
- Lead sponsor
- Cardiovascular Innovation and Research Institute
- NCT number
- NCT03428048
What you commit to
- Study type: Observational
- Planned participants: 1000
- From 1 Mar 2016 to the primary completion date, 31 Mar 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Candidates will be excluded from the study if any of the following conditions are present:
- Failure and / or inability and / or unwillingness to provide informed consent.
Other
- Likely problems, in the judgement of the investigators, with maintaining follow-up.
Who the study is looking for
- Candidates will be included in the study only if all the following conditions are met:
- Age \>18 years
- The subject has been informed of the nature of the study, agrees to its provisions, is able to comprehend, and has provided informed consent.
- The subject is available for follow-up.
- The subject has a diagnosis of coronary artery disease or Afib.
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Valley View Hospital Coordinator of this site? Confirm its status | Glenwood Springs | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.