MagnetOs Flex Matrix Compared to Trinity Elite Mixed With Local Autograft in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion
Sponsor: Kuros Biosurgery AG • ClinicalTrials.gov ID: NCT05037968
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This is a phase IV post-marketing study for MagnetOs Flex Matrix. MagnetOs Flex Matrix is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease and undergoing spinal fusion surgery. In this study, MagnetOs Flex Matrix will be used according to the latest U.S. Instructions For Use, specifically as a bone graft extender mixed with autograft in a 1:1 vol.% in the posterolateral spine. Trinity Elite will also be used according to its latest IFU approved in the US. Specifically, this cellular based allograft is an allograft intended for the treatment of musculoskeletal defects.
Interventions
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MagnetOs Flex Matrix
(Device)
Procedure: Instrumented Posterolateral Lumbar Fusion
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Trinity Elite
(Device)
Procedure: Instrumented Posterolateral Lumbar Fusion
Eligibility criteria
Conditions
Locations
- Hartford Hospital — Hartford, Connecticut, United States
- Central CT Neurosurgery & Spine — New Britain, Connecticut, United States
- Rush University Medical Center — Chicago, Illinois, United States
- MedStar Health Research Institute — Columbia, Maryland, United States
- Michigan Orthopedic Surgeons — Bloomfield Hills, Michigan, United States
- Pinehurst Surgical Clinic — Pinehurst, North Carolina, United States
- The Ohio State University — Columbus, Ohio, United States
- Huntsman Spinal Clinic — Salt Lake City, Utah, United States
- Inova Healthcare — Fairfax, Virginia, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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