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Follow-Up of the Prevision® Hip Stem

NCT04833634 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 46

Last updated 2022-11-18

No results posted yet for this study

Summary

The main objective of this study is to represent the treatment reality at the study site and to draw conclusions from cases of failure or suboptimal outcome. Potential risk factors for revision surgery, suboptimal outcome or radiologic sign of loosening, bone non-union or stem subsidence will be evaluated. Next to the functional outcome, stem subsidence will be used as an important indicator for a stable fixation of the revision stem.

Conditions

  • Periprosthetic Fracture Around Prosthetic Joint Implant
  • Aseptic Loosening of Prosthetic Joint

Sponsors & Collaborators

  • Aesculap AG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-14
Primary Completion
2022-06-13
Completion
2022-06-13

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 NCT04833634 on ClinicalTrials.gov