Registry Tracking Care and Outcomes for People Receiving Defibrillator Devices
Tracks people with heart failure or heart rhythm problems who receive implanted defibrillators.
Plain-language title generated from the registry record
Registry title: Implantable Cardioverter Defibrillator (ICD Registry)
Key facts
- Where
- Washington D.C., United StatesSee the site
Where in United States
- American College of Cardiology/National Cardiovascular Data Registry (NCDR)Washington D.C., United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- American College of Cardiology
- Trial code
- NCT01999140
- Record updated
- 18 April 2024
- Original description
The ICD Registry™ is a nationwide quality program that helps participating hospitals measure and improve care for patients receiving implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy devices with defibrillator (CRT-Ds). The ICD Registry captures the characteristics, treatments, and outcomes of patients receiving (ICDs). Patient-level data is submitted by participating hospitals on a quarterly basis to the American College of Cardiology Foundation's (ACCF) National Cardiovascular Data Registry (NCDR) which then produces an Outcomes Report of the hospital's data, with comparison to both a volume peer group (number of ICD patients submitted annually) and the entire ICD registry data set.Read full original descriptionShow less
Implantable Cardioverter Defibrillator (ICD Registry)
The ICD Registry™ is a nationwide quality program that helps participating hospitals measure and improve care for patients receiving implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy devices with defibrillator (CRT-Ds). The ICD Registry captures the characteristics, treatments, and outcomes of patients receiving (ICDs). Patient-level data is submitted by participating hospitals on a quarterly basis to the American College of Cardiology Foundation's (ACCF) National Cardiovascular Data Registry (NCDR) which then produces an Outcomes Report of the hospital's data, with comparison to both a volume peer group (number of ICD patients submitted annually) and the entire ICD registry data set.
Inclusion: All patients who receive an ICD/CRT-D (initial or generator change) for primary or secondary prevention purposes; All patients with an ICD/CRT-D undergoing a Lead Only procedure; U.S. populations must submit all patients who receive an ICD/CRT-D (initial or generator change) for primary prevention purposes who are insured by Medicare.
Exclusion: None.
All U.S and International patients.