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ACTIVE NOT RECRUITING

Cardiac Implantable Electronic Device (CIED) Research Study

NCT05061862 · View on ClinicalTrials.gov ↗

Study Summary

The study is designed to collect data on Cardiovascular Implantable Electronic Device (CIED) information, implant procedure details, and/or patient characteristics to support development of future CIED products and procedures.

Interventions

  • DEVICE cardiac implantable electronic devices (CIEDs)

Study Locations (9)

Virginia

  • University of Virginia Medical Center — Charlottesville
  • Inova Fairfax Hospital — Falls Church
  • Sentara Norfolk General Hospital — Norfolk

Pennsylvania

  • Lancaster General Hospital — Lancaster
  • Allegheny General Hospital — Pittsburgh

Florida

  • The Cardiac & Vascular Institute — Gainesville

Georgia

  • Georgia Arrhythmia Consultants — Macon

Oregon

  • Oregon Health & Science University Hospital — Portland

Other

  • UZ Leuven - Campus Gasthuisberg — Leuven

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2022-03-06
Est. Completion 2026-05-01

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05061862

The ClinicalTrials.gov registry entry for NCT05061862 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 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic Cardiac Rhythm and Heart Failure, which has 56 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Bradycardia appearing as the primary indexed condition, and to 1 intervention — of which cardiac implantable electronic devices (CIEDs) 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: NCT05061862 reports 9 study locations spanning 6 distinct geographic areas — top geographies include Virginia, Pennsylvania, Florida. 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 NCT05061862 about?

NCT05061862 is a clinical study titled "Cardiac Implantable Electronic Device (CIED) Research Study". The study is designed to collect data on Cardiovascular Implantable Electronic Device (CIED) information, implant procedure details, and/or patient characteristics to support development of future CIED products and procedures.

What is the current status of trial NCT05061862?

This trial is currently active not recruiting. The enrollment target is 1,000 participants. The study started on 2022-03-06. Estimated completion is 2026-05-01.

What conditions does trial NCT05061862 study?

This clinical trial studies the following conditions: Bradycardia, Arrhythmias, Cardiac, Tachycardia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05061862?

The interventions under investigation include: cardiac implantable electronic devices (CIEDs) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05061862?

This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, which has 56 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05061862 being conducted?

This trial has 9 study locations across Florida, Georgia, Oregon, Pennsylvania, Virginia. 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