The primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with patient specific rods. The secondary objective is to collect clinical and radiographic outcomes of patients with hardware as a control cohort to the patient-specific rods.
Patient has been/ will be operated and instrumented with patient-specific rod or spine hardware (control cohort)
Patient able to consent or assent
Patient unable to sign an informed consent form
Patient unable to complete a self-administered questionnaire
Patient is pregnant or planning on becoming pregnant during the duration of their study participation
Patient is older than 85
University of Colorado, Denver
Lead sponsor
Personalized Spine Study Group
Collaborator