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Clinical Trial Summary

This is a single centre, non-blinded safety trial. Patients undergoing lumbar fusion will be treated using patient specific guides (PSG) or navigation. Patients requiring lumbar fusion will be treated using conventional surgical methods except when inserting pedicle screws, where half of the patients will be having screws inserted using PSGs. The conventional method of navigation and intraoperative imaging will be used in conjunction with PSGs, to confirm the safety of the guide trajectory. The primary outcome will be screw accuracy measured in degrees from planned trajectory and mm from the planned entry point.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04751981
Study type Interventional
Source Lawson Health Research Institute
Contact
Status Not yet recruiting
Phase N/A
Start date February 2021
Completion date February 2023

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