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Recruiting NCT01999140

NCT01999140 Implantable Cardioverter Defibrillator (ICD Registry)

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Clinical Trial Summary
NCT ID NCT01999140
Status Recruiting
Phase
Sponsor American College of Cardiology
Condition Heart Failure
Study Type OBSERVATIONAL
Enrollment 1,750 participants
Start Date 2005-06
Primary Completion 2030-06

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 1,750 participants in total. It began in 2005-06 with a primary completion date of 2030-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

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 ICD/CRT-D (initial or generator change) for primary prevention purposes who are insured by Medicare. Exclusion Criteria: None

Contact & Investigator

Central Contact

NCDR Product Support

✉ ncdr@acc.org

📞 1-800-257-4737

Frequently Asked Questions

Who can join the NCT01999140 clinical trial?

This trial is open to participants of all sexes, studying Heart Failure. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT01999140 currently recruiting?

Yes, NCT01999140 is actively recruiting participants. Contact the research team at ncdr@acc.org for enrollment information.

Where is the NCT01999140 trial being conducted?

This trial is being conducted at Washington D.C., United States.

Who is sponsoring the NCT01999140 clinical trial?

NCT01999140 is sponsored by American College of Cardiology. The trial plans to enroll 1,750 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology