Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING

Personalized Therapy Study - HFRS (TriageHF) Post Approval Study

NCT04489225 · View on ClinicalTrials.gov ↗

Study Summary

Medtronic is sponsoring the HFRS PAS to evaluate the HFRS feature (TriageHF) when used in routine clinical practice following commercial release. The HFRS PAS is conducted within Medtronic's Product Surveillance Registry (PSR) platform.

Conditions Studied

Interventions

  • OTHER Observational

Study Locations (20)

Florida

  • Heart Rhythm Solutions — Hollywood
  • Baptist Health — Jacksonville
  • Cardiovascular Institute of Northwest Florida — Panama City
  • Heart & Vascular Institute of Florida — Safety Harbor
  • Heart Rhythm Consultants P.A. (Sarasota Memorial Research) — Sarasota

California

  • Chula Vista Cardiac Center — Chula Vista
  • Cardiovascular Consultants Medical Group — Van Nuys
  • Cardiology Associates Medical Group — Ventura

Colorado

  • Colorado Springs Cardiology — Colorado Springs
  • Denver Heart — Denver
  • Colorado Heart and Vascular, PC — Lakewood

Connecticut

  • Hartford Hospital — Hartford
  • Yale New Haven Hospital — New Have

Arizona

  • Southwest EP — Chandler

Arkansas

  • Saint Vincent Heart Clinic Arkansas — Little Rock

Indiana

  • Deaconess Specialty Physicians — Evansville

Iowa

  • Iowa Heart — Des Moines

Trial Details

FieldValue
Enrollment Target 2,200 participants
Start Date 2020-08-01
Est. Completion 2028-01-31

Sponsor

Medtronic

14 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04489225

The ClinicalTrials.gov registry entry for NCT04489225 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 2,200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic, which has 14 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 appearing as the primary indexed condition, and to 1 intervention — of which Observational 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: NCT04489225 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Florida, California, Colorado. 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 NCT04489225 about?

NCT04489225 is a clinical study titled "Personalized Therapy Study - HFRS (TriageHF) Post Approval Study". Medtronic is sponsoring the HFRS PAS to evaluate the HFRS feature (TriageHF) when used in routine clinical practice following commercial release. The HFRS PAS is conducted within Medtronic's Product Surveillance Registry (PSR) platform.

What is the current status of trial NCT04489225?

This trial is currently active not recruiting. The enrollment target is 2,200 participants. The study started on 2020-08-01. Estimated completion is 2028-01-31.

What conditions does trial NCT04489225 study?

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

What interventions are being tested in trial NCT04489225?

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

Who is sponsoring clinical trial NCT04489225?

This trial is sponsored by Medtronic, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04489225 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. 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