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Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System

Trauma Clinical Trial

Official title:
Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System

Clinical Trial Summary

The purpose of the study is to assess screw deviation from pre-planned trajectory using the Mazor X robotic system in patients undergoing posterior thoracolumbar arthrodesis procedures between T2-S1.

Clinical Trial Description

This trial will prospectively evaluate screw deviation from pre-planned trajectory using the standard of care Mazor X robotic system. Patients undergoing posterior thoracolumbar arthrodesis procedures utilizing pedicle screw instrumentation at previously uninstrumented levels for degenerative conditions, spinal deformity, spinal infection, trauma, or neoplastic processes between T2-S1 will be asked to participate in this prospective cohort study. This single centered study will enroll up to 50 patients to achieve a total number of 250 screws for assessment. Subjects will be followed till discharge following surgery. All subjects enrolled in the study will be recruited from a pool of subjects eligible for posterior thoracolumbar arthrodesis surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05884593
Study type Interventional
Source Ohio State University
Contact
Status Active, not recruiting
Phase N/A
Start date March 5, 2021
Completion date June 30, 2024
View Details
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