Registry Study of Personalized Spine Rods and Standard Spine Hardware Outcomes Tracking Clinical and Radiographic Results in Patients Aged 10 to 85

What this Trial Is About

Researchers are tracking clinical and radiographic results in patients who receive personalized spine rods or standard spine hardware for spinal conditions such as scoliosis, degenerative disc disease, and spinal fusion. This observational registry study aims to better understand patient outcomes, surgical implant effectiveness, and risks related to spinal surgery and hardware over time. Participants include those treated with patient-specific posterior spinal fusion rods or other spine hardware. The study follows patients through their usual care visits before and after surgery. During these visits, patient-reported questionnaires and spinopelvic measurements from routine X-rays will be collected to assess sagittal alignment and fusion status. Patients will be monitored over up to four years to observe rod curvature maintenance and postoperative complications. Data collection occurs during standard care visits with no extra treatments assigned. Researchers will analyze clinical outcomes and radiographic changes to evaluate hardware performance and patient recovery in different subgroups based on surgery type and health conditions.

Personalized Spine Study Group (PSSG) Registry