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NCT04679844 · ClinicalTrials.gov registry record · 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
A NA study of Degenerative Disc Disease and Back Pain, sponsored by Kuros Biosurgery.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 6
- Study locations
NCT04679844: Recruiting NA study of Degenerative Disc Disease and Back Pain, sponsored by Kuros Biosurgery.
NCT04679844 is a NA study of Degenerative Disc Disease and Back Pain that is actively recruiting participants, run by Kuros Biosurgery. The registered enrollment target is 60 participants, below the 167-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (64% lower). The trial reports 6 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04679844, a NA study of Degenerative Disc Disease and Back Pain, is actively recruiting participants, sponsored by Kuros Biosurgery.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 6
- Study locations
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.
Primary Outcome
The rate of posterolateral lumbar/thoracolumbar fusion assessed by CT-scan at Month 12. Radiographic as determined by evidence of bridging trabeculae or continuous bony connection between the superior and inferior transverse processes.
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2024-12-06 |
| Est. Completion | 2027-08-30 |
| Phase | NA |
What NCT04679844 shows while recruiting
NCT04679844 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 167-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (64% lower).
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.
NCT04679844 lists 6 locations in 6 states (California, Michigan, Missouri).
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.
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).
Who is sponsoring clinical trial NCT04679844?
This trial is sponsored by Kuros Biosurgery, which has 4 total clinical trials registered on ClinicalTrials.gov.
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.
Learn More About Clinical Trials
Similar trials for Degenerative Disc Disease
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT04679844's enrollment target sits among peer trials
60 26th of 42 higher than 16 of 42 other Degenerative Disc Disease trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Degenerative Disc Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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