Implantable Cardioverter Defibrillator (ICD Registry)
Recruiting
Observational Study
Heart Failure
Nonischemic Cardiomyopathy
Ischemic Cardiomyopathy
Ventricular Arrhythmia
Complications; Device, Cardiac
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,750 (estimated)
- Sponsor
- American College of Cardiology · Other
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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 particip…
Trial Locations
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Eligibility Criteria
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 …
Contacts