Implantable Cardioverter Defibrillator (ICD Registry)

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
American College of Cardiology
Study ID
NCT01999140
Status
Recruiting

Conditions

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

Eligibility Criteria

Sex
ALL
Age
N/A - N/A
Healthy Volunteers
Not accepted

Study Details

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 Dates

Start date
Jun 30, 2005
Status verified
Apr 2024
Primary completion
Jun 30, 2030
Completion
Jun 30, 2030

Study Design

Enrollment
1,750 participants (estimated)

Arms

  • Arm: Primary prevention

Primary Outcome Measure

Risk Adjusted Complications and Death Composite Measure [ Time Frame: Post-procedure until discharge occurences. Reported quarterly based on a rolling 1 year of data. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
American College of Cardiology/National Cardiovascular Data Registry (NCDR)Washington D.C.District of Columbia20037
NCDR Product Support
800-257-4737

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