100
Participants
Start Date
November 19, 2021
Primary Completion Date
October 1, 2025
Study Completion Date
April 1, 2026
Medtronic Adaptix™ titanium implants
Patients who will be having a spinal fusion procedure as part of their standard of care treatment will be randomized to receive either the Medtronic titanium or the PEEK cage supplemented with a pedicle screw system and milled local autograft bone supplemented with GRAFTON DBM DBF. In order to assess fusion, patients will undergo a research-only CT Scan at 6 months post-surgery.
Medtronic CAPSTONE® PEEK cage
Medtronic CAPSTONE® PEEK cage
The Ohio State University Wexner Medical Center Neurological Surgery, Columbus
Ohio State University
OTHER