An observational study in Osteoarthritis, Knee, sponsored by Spokane Joint Replacement Center. Completed at 1 site in United States. Open to participants aged 20 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-12-13.
Sponsored by Spokane Joint Replacement Center · Observational
This study compares the clinical and radiographic outcomes obtained with the use of the Stryker Triathalon® Cruciate Substituting (CS) and Posterior Stabilized (PS) tibial inserts.
4,398 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.
This study's enrollment of 125 is above the median of 100 across 791 observational studies indexed under Osteoarthritis.
Browse Osteoarthritis studies →Spokane Joint Replacement Center is the lead sponsor of 5 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Adult patients undergoing total knee arthroplasty
Exclusion Criteria:
Other criteria may apply
Device: Stryker Triathlon® CS Tibial Insert
Device: Stryker Triathlon® PS Tibial Insert
Clinical outcomes, Knee Society Score
Clinical outcomes to include overall success, failure rate, revison rate, clinical scores (Knee Society Score), range of motion, pain, stability, radiographic success
Time frame: Pre-operative, 6 weeks, 6 months, 1, 2, 3, 4, and 5 years post-operative
This study is completed, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.
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Spokane Joint Replacement Center