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Randomised Controlled Trial PFC Versus CKS Total Knee Prostheses

Conditions
Osteoarthritis, Knee
Registration Number
NCT00228137
Lead Sponsor
Radboud University Medical Center
Brief Summary

The purpose of this study is to compare the functional outcome of two different total knee prostheses in a prospective randomised study.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
90
Inclusion Criteria

All patients on the waiting list for a TKA due to an invalidating gonarthrose as a result of osteo-arthrosis or secondary to a rheumatic disease or a trauma.

Exclusion Criteria
  • patient suffering from juvenile rheumatic disease
  • patient suffering hemophilia
  • patient on the waiting list for posterior stabilized TKA or hinge joint.
  • patient who suffers from a lesion of the ligaments due to surgery
  • patient who is legally not capable to make decisions
  • patient who suffer from cancer

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UMC Radboud

🇳🇱

Nijmegen, Netherlands

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