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Clinical Trials/NL-OMON36423
NL-OMON36423
Not yet recruiting
Not Applicable

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

Academisch Medisch Centrum0 sites42 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
cartilage damage
Sponsor
Academisch Medisch Centrum
Enrollment
42
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
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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