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Study identifier: NCT06209684 Synced from ClinicalTrials.gov · July 28, 2026
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Carbofix Pedicle Screw System: Evaluation of the Clinical and Radiographic Outcomes of the Use of a Carbon Fiber Device Compared to Titanium Devices in Patients Undergoing Spinal Arthrodesis for Degenerative Spinal Diseases

Condition: Degenerative Disc Disease  ·  Sponsor: Istituto Ortopedico Rizzoli

PhaseNA
Planned participants118
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Previous clinical study carried out on cancer patients at IOR Spine Surgery (approved in October 2014). The carbon device is indicated in patients suffering from vertebral tumors who need stabilization and will then carry out radiotherapy, because carbon has a practically zero level of interference with ionizing radiation. Carbon also allows for better visualization of the implants on MRI/CT and X-ray. There are no studies in the literature analyzing the use of carbon fiber devices in lumbar degenerative pathologies. 118 patients suffering from degenerative spinal pathology requiring 1 or 2 levels of lumbar or lumbosacral fusion will be valutated.

This description comes directly from the study's public registry record.

Talk to the study team

Alessandro Gasbarrini, MD  ·  0516366  ·  alessandro.gasbarrini@ior.it

Cristiana Griffoni, PhD  ·  0516366  ·  cristiana.griffoni@ior.it

Always discuss trial participation with your own doctor first.

Locations (1)

Istituto Ortopedico RizzoliBologna, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06209684