Recruiting

ICD Registry

Sponsor:

American College of Cardiology

Code:

NCT01999140

Conditions

Heart Failure

Nonischemic Cardiomyopathy

Ischemic Cardiomyopathy

Ventricular Arrhythmia

Complications; Device, Cardiac

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Study Details

Brief 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.

Conditions

Heart Failure

Nonischemic Cardiomyopathy

Ischemic Cardiomyopathy

Ventricular Arrhythmia

Complications; Device, Cardiac

Study ID

NCT01999140

Start date

Jun, 2005

Status verified date

Apr, 2024

Completion date

Jun, 2030

Anticipated

Primary completion date

Jun, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

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 ICD/CRT-D (initial or generator change) for primary prevention purposes who are insured by Medicare.

Exclusion Criteria:

None

Study Design

Enrollment

1750 participants

Anticipated

Interventions and Outcome Measures

Arms

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 and Locations

Central contacts

NCDR Product Support

1-800-257-4737ncdr@acc.org

Locations

American College of Cardiology/National Cardiovascular Data Registry (NCDR)

Recruiting

Washington, District of Columbia, United States, 20037

Contacts

NCDR Product Support

800-257-4737ncdr@acc.org

More Information

Sponsor

American College of Cardiology

Last update posted

Apr 18, 2024

Last verified

Apr, 2024

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by American College of Cardiology on 2024-04-18.