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RECRUITING

Role of Novel ILR in the Management of PVCs

NCT06060548 · View on ClinicalTrials.gov ↗

Study Summary

This prospective, observational study is a single center clinical registry of patients referred for management of symptomatic or asymptomatic Premature Ventricular Contractions (PVCs). Subjects will be followed through 12 months. The study will enroll approximately 50 patients.

Interventions

  • OTHER Monitoring of patients presenting with PVCs

Study Locations (6)

Missouri

  • Centerpoint Medical Center Clinic — Independence
  • Centerpoint Medical Center — Independence
  • Research Medical Center Clinic — Kansas City
  • Research Medical Center — Kansas City

Kansas

  • Kansas City Heart Rhythm Institute - Roe Clinic — Overland Park
  • Overland Park Regional Medical Center — Overland Park

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-04-20
Est. Completion 2025-12

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06060548

The ClinicalTrials.gov registry entry for NCT06060548 describes a study currently listed as 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 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kansas City Heart Rhythm Research Foundation, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Myocarditis appearing as the primary indexed condition, and to 1 intervention — of which Monitoring of patients presenting with PVCs 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: NCT06060548 reports 6 study locations spanning 2 distinct geographic areas — top geographies include Missouri, Kansas. 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 NCT06060548 about?

NCT06060548 is a clinical study titled "Role of Novel ILR in the Management of PVCs". This prospective, observational study is a single center clinical registry of patients referred for management of symptomatic or asymptomatic Premature Ventricular Contractions (PVCs). Subjects will be followed through 12 months. The study will enroll approximately 50 patients.

What is the current status of trial NCT06060548?

This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2022-04-20. Estimated completion is 2025-12.

What conditions does trial NCT06060548 study?

This clinical trial studies the following conditions: Myocarditis, PVC - Premature Ventricular Contraction. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06060548?

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

Who is sponsoring clinical trial NCT06060548?

This trial is sponsored by Kansas City Heart Rhythm Research Foundation, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06060548 being conducted?

This trial has 6 study locations across Kansas, Missouri. 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