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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cruciate Substituting Tibial Insert |
| ||
| Posterior Stabilized Tibial Insert |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Stryker Triathlon® CS Tibial Insert | Device |
| ||
| Stryker Triathlon® PS Tibial Insert |
| Measure | Description | Time Frame |
|---|---|---|
| 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 | Pre-operative, 6 weeks, 6 months, 1, 2, 3, 4, and 5 years post-operative |
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Inclusion Criteria:
Exclusion Criteria:
Other criteria may apply
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Adult patients undergoing total knee arthroplasty
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| Name | Affiliation | Role |
|---|---|---|
| David F Scott, MD | Spokane Joint Replacement Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Spokane Joint Replacement Center | Spokane | Washington | 99218 | United States |
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| ID | Term |
|---|---|
| D020370 | Osteoarthritis, Knee |
| D010003 | Osteoarthritis |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
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| Device |
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