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
- NCDR Product Support1-800-257-4737
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| American College of Cardiology/National Cardiovascular Data Registry (NCDR) | Washington D.C. | District of Columbia | 20037 |
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