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Clinical Trials/NL-OMON42998
NL-OMON42998
Completed
N/A

Inducible Displacement in Total Knee Prostheses - Inducible Displacement

eids Universitair Medisch Centrum0 sites30 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
aseptic loosening
Sponsor
eids Universitair Medisch Centrum
Enrollment
30
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients will be included if
  • they underwent TKR for primary as well as secondary gonarthrosis as long as the indication for surgery is clearly specified
  • a minimal set of patient characteristics (age, gender, BMI, co\-morbidity) and disease characteristics (radiological severity, knee function and alignment, status of other knee or hip joints, previous surgeries of the affected knee) is available.
  • they are at least \*up to date\* in terms of follow\-up of their respective study (i.e. the most recent examination was less than a year ago and patients have a post\-operative examination)
  • they participated for at least three years in their respective study and have a usable MTPM\-value (i.e. \>\= 3 bone\-markers can be consistently matched with the reference\-examination with a CN \< 120 over the most recent two years of follow\-up
  • their standard RSA data meets the criteria as mentioned in the ISO\-standard
  • they are willing to participate and able to perform the 4 pre\-set tasks for the inducible displacement measurements

Exclusion Criteria

  • Patients will be excluded from participation if they do not meet the inclusion criteria, or if they already underwent revision surgery of their TKR since the start of the study they were enrolled in.

Outcomes

Primary Outcomes

Not specified

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