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

NCT05884593 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-08-12

No results posted yet for this study

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.

Conditions

  • Spinal Deformity
  • Spinal Infection
  • Trauma
  • Neoplastic Processes
  • Degenerative Spinal Conditions

Interventions

DEVICE

Pedicle screw instrumentation using Mazor X robotic system

Pedicle screw instrumentation using Mazor X robotic system

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY
  • Ohio State University

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-05
Primary Completion
2023-12-31
Completion
2025-12-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05884593 on ClinicalTrials.gov