Proprio Spine Measurement Tool
NCT: NCT07023393 · WITHDRAWN
Brief Summary
This study will prospectively collect data to evaluate the effectiveness of a novel intraoperative spinal measurement system to assist the surgeon with intraoperatively achieving pre-planned alignment-related parameters to the patient's spine. The study will also collect outcomes data to determine if achievement of these spinal alignment-related parameters result in satisfactory outcomes and if it reduces the rate of secondary surgeries. Objectives Primary: To evaluate the effectiveness of a novel intraoperative spinal measurement system to assist the surgeon with achieving the surgeon's preplanned alignment-related parameters intraoperatively. Secondary: To determine if there is a correlation between 1) achievement of preoperative planned alignment-related parameters intraoperatively, and 2) outcomes. Hypothesis The application of the intraoperative spinal measurement tool for patients undergoing spinal fusion surgery will improve the surgeon's ability to achieve pre-planned alignment-related parameters intraoperatively and doing so will provide improved outcomes.
Frequently Asked Questions
What is Proprio Spine Measurement Tool?
Proprio Spine Measurement Tool is a clinical trial registered under NCT07023393. Current status: WITHDRAWN.
What is the status of NCT07023393?
The current status of NCT07023393 (Proprio Spine Measurement Tool) is: WITHDRAWN.
When did Proprio Spine Measurement Tool start?
Proprio Spine Measurement Tool started on 2026-04-20.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.