Back to search results
NCT06686017

Virtuos Bone Graft in Lumbar Fusion

Enrolling by Invitation
Not specifiedAges 18+Observational
Orthofix Inc.
~150 participants
Updated 2025-11-28 on ClinicalTrials.gov

At a glance

Recruiting sites
0 of 9 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Fusion
Measured over 12-months

Conditions

Degenerative Disc Disease

Explore related trials

Fusion of lateral lumbar interbodyInterbody fusion of lumbar spine by anterior approachIntervertebral Disc Degenerative DisorderLumbar spinal fusion

NCT06686017

Where you'd take part

This study runs at 9 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Lowcountry Orthopaedics and Sports Medicine

    North Charleston, South Carolinano site contact published

  • Michigan Orthopedic Surgeons

    Southfield, Michiganno site contact published

  • Northern Rockies Orthopaedics

    Missoula, Montanano site contact published

  • OrthoSC

    Myrtle Beach, South Carolinano site contact published

  • Pinehurst Surgical Clinic

    Pinehurst, North Carolinano site contact published

  • South Bend Orthopaedics

    South Bend, Indianano site contact published

  • South Carolina Sports Medicine

    North Charleston, South Carolinano site contact published

  • Tuckahoe Orthopaedics

    Richmond, Virginiano site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Want this trial checked against your situation?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Subject must undergo lumbar interbody fusion study at 1-2 contiguous levels.
Virtuos must be the primary bone graft (≥ 50% of the total graft volume) and may be augmented with autograft or cortical or cancellous bone chips.
Subject must be willing and able to sign an informed consent document.
Subject must be willing and able to return for all follow-up visits, agree to participate in postoperative clinical and radiographic evaluations, and comply with the required study protocol.-

Exclusion

Subject is under 18 years of age (\<18) at the time of consent.
Subject has had prior lumbar spine fusion surgery at any level.
Subject has greater than grade 1 spondylolisthesis of the lumbar spine. Subject is currently undergoing treatment for malignancy or has undergone treatment for malignancy in the past 5 years (benign skin cancer is permitted)
Subject has an active local or systemic infection or is undergoing adjunctive treatment for local or systemic infection

What this trial measures

  • Fusion12-months

    Fusion of the spinal motion segments