This trial is active, not recruiting.

Condition osteoarthritis, knee
Sponsor Radboud University
Start date November 2002
End date November 2012
Trial size 90 participants
Trial identifier NCT00228137, FBW STRATEC 96856, HJM25577


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

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model defined population
Time perspective longitudinal

Eligibility Criteria

Male or female participants of any age.

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

Additional Information

Official title A Prospective Randomized Double-Blind Study to Assess the Functional Differences Between the PFC and CKS Knee Prostheses
Trial information was received from ClinicalTrials.gov and was last updated in August 2007.
Information provided to ClinicalTrials.gov by Radboud University.