Implantable Cardioverter Defibrillator (ICD Registry)
American College of Cardiology
1,750 participants
Jun 1, 2005
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria4
- All U.S and International patients.
- 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 Criteria1
- None
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT01999140