RECRUITINGOBSERVATIONAL
Implantable Cardioverter Defibrillator (ICD Registry)
About This Trial
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 May Be Eligible (Plain English)
All U.S and International patients.
Who May Qualify:
- 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.
Who Should NOT Join This Trial:
None
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
All U.S and International patients.
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
Locations (1)
American College of Cardiology/National Cardiovascular Data Registry (NCDR)
Washington D.C., District of Columbia, United States