Implantable Cardioverter Defibrillator (ICD Registry)

Recruiting now

Conditions studied: Heart Failure, Nonischemic Cardiomyopathy, Ischemic Cardiomyopathy, Ventricular Arrhythmia, Complications; Device, Cardiac

In brief

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.

Key facts

Study ID

NCT01999140

Run by

American College of Cardiology

People needed

1750

Starts

2005-06-01

Expected to finish

2030-06-01

Last updated by the study team

2024-04-18

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• None

Where it is running

• American College of Cardiology/National Cardiovascular Data Registry (NCDR) — Washington D.C., District of Columbia, United States (enrolling)

Full record on ClinicalTrials.gov

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