Implantable Cardioverter Defibrillator (ICD Registry)

Heart Failure Clinical Trial

Official title: Implantable Cardioverter Defibrillator (ICD Registry)

Status Recruiting

Clinical Trial 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.

Clinical Trial Description

In January 2005 the Centers for Medicare and Medicaid Services (CMS) expanded the covered indications for primary prevention implantable cardioverter defibrillators (ICDs) to incorporate the findings from the Sudden Cardiac Death Heart Failure Trial (SCDHeFT) and the Multicenter Automatic Defibrillator Implantation Trial II (MADIT II). As part of this expansion, CMS mandated that a national registry be formed to compile data on Medicare patients implanted with primary prevention ICDs to confirm the appropriateness of ICD utilization in this patient population. Responding to this mandate, a collaborative effort of the Heart Rhythm Society (HRS)and the American College of Cardiology Foundation (ACCF), utilizing the expertise of the National Cardiovascular Data Registry (NCDR®), developed the ICD Registry™. Enrollment opened on June 1, 2005. CMS selected the NCDR ICD Registry as the mandated national registry in October 2005. ;

Related Conditions & MeSH terms

• Cardiomyopathies
• Complications; Device, Cardiac
• Heart Failure
• Ischemic Cardiomyopathy
• Nonischemic Cardiomyopathy
• Ventricular Arrhythmia

• NCT number: NCT01999140
• Study type: Observational [Patient Registry]
• Source: American College of Cardiology
• Contact: NCDR Product Support
• Phone: 1-800-257-4737
• Email: ncdr@acc.org
• Status: Recruiting
• Start date: June 2005
• Completion date: June 2030