Implantable Cardioverter Defibrillator (ICD Registry)
Recruiting · NCT01999140 · Observational (researchers observe without assigning treatment) · Lead sponsor: American College of Cardiology
View the official record on ClinicalTrials.gov →What this trial is about
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.
Who can take part
Inclusion criteria
- 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 criteria
- None
Where it is running
1 location listed across 1 US state.
- American College of Cardiology/National Cardiovascular Data Registry (NCDR) - Washington D.C., District of Columbia, United States