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RECRUITING NA

Comparative Effectiveness of Prophylactic ICD Versus Non-ICD Therapy

NCT06543446 · View on ClinicalTrials.gov ↗

Study Summary

The investigators aim to compare the risk of mortality of Non-implantable carioverter defibrillator (ICD) vs. ICD management in patients with heart failure with reduced ejection fraction (HFrEF).

Interventions

  • PROCEDURE ICD implantation

Study Locations (15)

New York

  • Northwell Health — New York
  • Nuvance Health Hudson Valley Cardiovascular Practice, PC — Poughkeepsie
  • University of Rochester — Rochester

New Jersey

  • Rutgers — New Brunswick
  • The Valley Hospital — Paramus

Alberta

  • University of Calgary — Calgary
  • University of Alberta — Edmonton

Maine

  • MaineHealth — Portland

Maryland

  • Johns Hopkins University — Baltimore

Massachusetts

  • Tufts Medical Center — Boston

Michigan

  • Corewell Health — Grand Rapids

Minnesota

  • Minneapolis Heart Institute Foundation — Minneapolis

Trial Details

FieldValue
Enrollment Target 3,290 participants
Start Date 2025-03-04
Est. Completion 2031-02-28
Phase NA

Sponsor

University of Rochester

437 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06543446

The ClinicalTrials.gov registry entry for NCT06543446 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 3,290 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 437 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Heart Failure With Reduced Ejection Fraction appearing as the primary indexed condition, and to 1 intervention — of which ICD implantation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06543446 reports 15 study locations spanning 11 distinct geographic areas — top geographies include New York, New Jersey, Alberta. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06543446 about?

NCT06543446 is a clinical study titled "Comparative Effectiveness of Prophylactic ICD Versus Non-ICD Therapy". The investigators aim to compare the risk of mortality of Non-implantable carioverter defibrillator (ICD) vs. ICD management in patients with heart failure with reduced ejection fraction (HFrEF).

What is the current status of trial NCT06543446?

This trial is currently recruiting. It is a NA study. The enrollment target is 3,290 participants. The study started on 2025-03-04. Estimated completion is 2031-02-28.

What conditions does trial NCT06543446 study?

This clinical trial studies the following conditions: Heart Failure With Reduced Ejection Fraction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06543446?

The interventions under investigation include: ICD implantation (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06543446?

This trial is sponsored by University of Rochester, which has 437 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06543446 being conducted?

This trial has 15 study locations across Maine, Maryland, Massachusetts, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial