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Clinical Trials/NL-OMON44792
NL-OMON44792
Completed
N/A

ncemented tibial component fixation in total knee replacement using porous titanium. A Randomized RSA Study - Uncemented tibia fixation in total knee replacement

Academisch Medisch Centrum0 sites42 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
cartilage damage
Sponsor
Academisch Medisch Centrum
Enrollment
42
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
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients diagnosed with osteoarthritis or rheumatoid arthritis of the knee requiring primary total knee arthroplasty
  • Patients capable of giving Informed Consent and expressing willingness to comply with the post\-operative follow\-up program
  • Patients having no major deformities, i.e. sagittal and coronal deformities are less than 15 degrees

Exclusion Criteria

  • Patients requiring revision arthroplasty
  • Patients unable or unwilling to sign the Patient Informed Consent specific to this study
  • Patients with osteoporosis of the tibial plateau
  • Patients with functional impairment of any other lower extremity joint besides the operated knee
  • Patients having a flexion contracture of 15° and more
  • Patients having a varus or valgus contracture of 15° and more
  • Patients having insufficient understanding of Dutch language to participate
  • Patients incompetent to fill in the clinical scores

Outcomes

Primary Outcomes

Not specified

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