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Comparison Between Exactech Guided Personalized Surgery (GPS) and Conventional Instrumentation of Shoulder Arthroplasty

NCT05615259 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 260

Last updated 2025-02-28

No results posted yet for this study

Summary

The primary objective of this study is to examine the optimization of Reverse Shouder Arthroplasty implant position between GPS and conventional techniques. The secondary objective is to assess the effect of implant position using GPS vs. conventional techniques on ROM and patient reported outcomes. Long-term follow-up to 10 years with minimum 2 year follow-up for patients.

Conditions

  • Technology
  • Comparison

Sponsors & Collaborators

  • Exactech

    lead INDUSTRY

Principal Investigators

  • Robert J Hillen, MD · Dijklander Ziekenhuis

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-23
Primary Completion
2030-12-31
Completion
2031-09-30

Countries

  • 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 NCT05615259 on ClinicalTrials.gov