Study of Clinical Outcomes After Spine Surgery Using Stryker Devices for Cervical, Thoracolumbar, and Spinal Deformity Conditions with 24-Month Follow-Up

What this Trial Is About

This research aims to collect data on the performance and safety of various Stryker spinal devices used in surgeries for conditions like degenerative disc disease and degenerative scoliosis. The study includes multiple protocols focused on different spine regions and conditions, monitoring patients over a 24-month period after device implantation. Participants undergo surgery with Stryker devices following the device-specific cleared instructions and surgical guides. The study consists of a master protocol and three sub-protocols targeting cervical, thoracolumbar, and adult spinal deformity conditions. Each sub-protocol has specific performance endpoints and hypotheses, with data collected on device function and safety throughout the study. Participants will provide patient-reported questionnaires at designated times, while researchers collect radiographic data and safety information during the 24 months following surgery. The study tracks outcomes from baseline through surgery and up to two years post-operation, aiming to understand device performance and patient safety over time.

Clinical Outcome Measure at Stryker Spine