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RECRUITING NA

Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion

NCT04679844 · View on ClinicalTrials.gov ↗

Study Summary

This is a phase IV post-marketing study for MagnetOs Easypack Putty. MagnetOs Easypack Putty is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease or spinal trauma undergoing spinal fusion surgery. In this study, MagnetOs Easypack Putty will be used according to the latest U.S. Instructions For Use, standalone in the posterolateral spine.

Interventions

  • DEVICE MagnetOs Easypack Putty
  • DEVICE Demineralized Bone Matrix or Fibers mixed with local autograft bone

Study Locations (6)

California

  • The Regents of the University of California- Irvine Campus — Irvine

Michigan

  • Corewell Health — Grand Rapids

Missouri

  • The Washington University — St Louis

Pennsylvania

  • Rothman Orthopaedic Institute — Philadelphia

Tennessee

  • Tennessee Orthopaedic Alliance — Nashville

Washington

  • University of Washington — Seattle

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2024-12-06
Est. Completion 2027-08-30
Phase NA

Sponsor

Kuros Biosurgery

30 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04679844

The ClinicalTrials.gov registry entry for NCT04679844 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 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kuros Biosurgery, which has 30 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 Degenerative Disc Disease appearing as the primary indexed condition, and to 2 interventions — of which MagnetOs Easypack Putty 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: NCT04679844 reports 6 study locations spanning 6 distinct geographic areas — top geographies include California, Michigan, Missouri. 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 NCT04679844 about?

NCT04679844 is a clinical study titled "Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion". This is a phase IV post-marketing study for MagnetOs Easypack Putty. MagnetOs Easypack Putty is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease or spinal trauma undergoing spinal fusion surgery. In this study, Mag...

What is the current status of trial NCT04679844?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-12-06. Estimated completion is 2027-08-30.

What conditions does trial NCT04679844 study?

This clinical trial studies the following conditions: Degenerative Disc Disease, Back Pain, Spine Fusion. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04679844?

The interventions under investigation include: MagnetOs Easypack Putty (DEVICE), Demineralized Bone Matrix or Fibers mixed with local autograft bone (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04679844?

This trial is sponsored by Kuros Biosurgery, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04679844 being conducted?

This trial has 6 study locations across California, Michigan, Missouri, Pennsylvania, Tennessee. 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