RECRUITING

Implantable Cardioverter Defibrillator (ICD Registry)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Implantable Cardioverter Defibrillator (ICD Registry)

Quick Facts

Study Start:2005-06
Study Completion:2030-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT01999140

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * All patients who receive an ICD/CRT-D (initial or generator change) for primary or secondary prevention purposes.
  2. * All patients with an ICD/CRT-D undergoing a Lead Only procedure.
  3. * 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.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

NCDR Product Support
CONTACT
1-800-257-4737
ncdr@acc.org

Study Locations (Sites)

American College of Cardiology/National Cardiovascular Data Registry (NCDR)
Washington, District of Columbia, 20037
United States

Collaborators and Investigators

Sponsor: American College of Cardiology

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2005-06
Study Completion Date2030-06

Study Record Updates

Study Start Date2005-06
Study Completion Date2030-06

Terms related to this study

Additional Relevant MeSH Terms

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