Implantable Cardioverter Defibrillator (ICD Registry)

Status: Recruiting
Location: See location...
Study Type: Observational
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.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• 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.

Locations
United States
Washington, D.c.
American College of Cardiology/National Cardiovascular Data Registry (NCDR)
RECRUITING
Washington D.c.
Contact Information
Primary
NCDR Product Support
ncdr@acc.org
1-800-257-4737
Time Frame
Start Date: 2005-06
Estimated Completion Date: 2030-06
Participants
Target number of participants: 1750
Treatments
Primary prevention
Related Therapeutic Areas
Sponsors
Leads: American College of Cardiology

This content was sourced from clinicaltrials.gov