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The European Robotic Spinal Instrumentation (EUROSPIN) Study

NCT03398915 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 932

Last updated 2026-03-31

Study results available
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Summary

In a multinational prospective study, preoperative, intraoperative, perioperative and follow-up data on patients receiving thoracolumbar pedicle screw placement for degenerative disease or infections or tumors will be collected. The three arms consist of robot-guided (RG), navigated (NV), or freehand (FH) screw insertion.

Conditions

  • Degenerative Disc Disease
  • Spondylolisthesis
  • Spinal Stenosis
  • Recurrent Disc Herniation
  • Spondylodiskitis
  • Spinal Tumor
  • Spinal Metastases

Interventions

PROCEDURE

Transpedicular Instrumentation

Transpedicular screw placement and instrumentation

Sponsors & Collaborators

  • University Hospital, Zürich

    collaborator OTHER

  • Marc Schröder

    lead OTHER

Principal Investigators

  • Victor E Staartjes, MD, PhD · Department of Neurosurgery, University Hospital Zurich

  • Granit Molliqaj, MD · Department of Neurosurgery, Hôpitaux Universitaires de Genève

  • Enrico Tessitore, MD · Department of Neurosurgery, Hôpitaux Universitaires de Genève

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2026-01-30
Completion
2026-05-01

Countries

  • Austria
  • France
  • Germany
  • Italy
  • Netherlands
  • Spain
  • Switzerland

Study Locations

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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 NCT03398915 on ClinicalTrials.gov