Degenerative Disc Disease Clinical Trial
Official title:
Personalized Spine Study Group Registry
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
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