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Quintex® Follow-up After One Year Minimum

NCT04489394 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2024-04-09

No results posted yet for this study

Summary

Prospective study, not randomised, non-interventional, monocentric, investigating an intended patient cohort of 60 patients already operated on the cervical spine due to degenerative disc disease of the cervical spine down to the first thoracolumbar VBR (C2-T1), who received a Quintex plate for stabilisation

Conditions

  • Degenerative Disc Disease
  • Spondylolisthesis
  • Trauma
  • Spinal Stenosis
  • Deformity of Spine
  • Pseudoarthrosis of Spine
  • Cervical Spondylosis
  • Instability; Back

Sponsors & Collaborators

  • Aesculap AG

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-11
Primary Completion
2020-02-18
Completion
2020-02-18

Countries

  • Germany

Study Locations

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Entities

Diseases

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 NCT04489394 on ClinicalTrials.gov