πŸ›οΈ Verified NIH Record β€’ Updated 2024-04-17

Implantable Cardioverter Defibrillator (ICD Registry) (NCT01999140)

🟒 Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: American College of Cardiology

🩺 Plain-English Summary (8th-Grade Level)

The ICD Registryβ„’ 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.

Who can join: Review the eligibility criteria below.

Location: American College of Cardiology/National Cardiovascular Data Registry (NCDR) β€” Washington D.C., District of Columbia

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • American College of Cardiology/National Cardiovascular Data Registry (NCDR) β€” Washington D.C., District of Columbia

πŸ“ž Contact the Study Coordinator

Phone: (800) 257-4737

Email: ncdr@acc.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Heart Failure clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—