As a registry, the primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with Medicrea's PSR. The secondary objective is to collect clinical and radiographic outcomes of patients with Medicrea hardware as a control cohort to the patient-specific rods.
The registry will follow the patient during their standard of care visits. At each visit, the patient will answer questions about themselves and also fill out patient reported outcome sheets. Spinopelvic measurements will be obtained on the x-rays taken. This registry is observational only, and there is no driving hypothesis for data collection. Some broad topics of discussion are: 1. Outcomes of patients sagittal profile through the pre-operative, plan and post-operative events 2. Effectiveness of rod in conjunction with other surgical implants by measurements of fusion assessment and sagittal alignment 3. Outcomes of patients in subgroups as defined by surgery performed, comorbidities, radiographic measurement, or other outcome variables 4. Rod curvature maintenance over the follow-up period 5. Understand the post-operative risks and complications from the pre-operative condition
Study Type
OBSERVATIONAL
Posterior spinal fusion rod
Data collection initiative
The study will collect clinical and radiographic outcomes of patients implanted with Medicrea's PSR.
Time frame: Up to 4 years
Collect clinical and radiographic outcomes of patients with Medicrea hardware
A control cohort to the patient-specific rods
Time frame: 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.