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Long Term Follow-up After Primary or Revision Shoulder Arthroplasty With a Patient- Specific Glenius Implant

NCT03806881 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2024-03-13

No results posted yet for this study

Summary

This post-market follow-up study investigates improvement in clinical and radiological outcome after reversed total shoulder arthroplasty with the patient-specific Glenius Glenoid Reconstruction system

Conditions

  • Arthroplasty, Replacement, Shoulder
  • Glenoid Cavity
  • Osteoarthritis of the Shoulder

Interventions

DEVICE

reversed glenoid prothesis

All patients will undergo a primary or revision arthroplasty with Glenius according to the routine practice at the investigation site and will be followed at specified visiting moments, during which radiological and clinical data will be gathered.

Sponsors & Collaborators

  • Materialise

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-01
Primary Completion
2024-10-01
Completion
2028-12-01

Countries

  • Belgium
  • Netherlands

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 NCT03806881 on ClinicalTrials.gov