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A Safety Study on Posterior Pedicle Screw System

NCT05821920 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2024-05-01

No results posted yet for this study

Summary

The goal of this study is to assess the MUST MINI system safety in patient who will undergo a posterior cervical spine fusion intervention. Patients will be invited to partecipate during preoperative visit and follow the postoperative visits according to the standard practice.

Conditions

  • Degenerative Disc Disease
  • Trauma Injury
  • Tumor

Interventions

DEVICE

MUST MINI system

cervical posterior fixation system

Sponsors & Collaborators

  • Medacta International SA

    lead INDUSTRY

Principal Investigators

  • Jens Lehmberg, Prof Med · München Klinik Bogenhausen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-28
Primary Completion
2023-06-28
Completion
2025-06-28
FDA Device
Yes

Countries

  • Germany

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 NCT05821920 on ClinicalTrials.gov