Stryker Triathlon® Cruciate Substituting vs. Posterior Stabilized Outcomes Study
NCT ID: NCT01367925
Last Updated: 2017-12-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
125 participants
OBSERVATIONAL
2007-12-31
2016-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Cruciate Substituting Tibial Insert
Stryker Triathlon® CS Tibial Insert
Posterior Stabilized Tibial Insert
Stryker Triathlon® PS Tibial Insert
Interventions
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Stryker Triathlon® CS Tibial Insert
Stryker Triathlon® PS Tibial Insert
Eligibility Criteria
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Inclusion Criteria
* Body mass index \<40
* Undergoing primary total knee arthroplasty for osteoarthritis of the knee
Exclusion Criteria
* Revisions
Other criteria may apply
20 Years
80 Years
ALL
Yes
Sponsors
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Spokane Joint Replacement Center
OTHER
Responsible Party
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David F. Scott, MD
PI
Principal Investigators
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David F Scott, MD
Role: PRINCIPAL_INVESTIGATOR
Spokane Joint Replacement Center
Locations
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Spokane Joint Replacement Center
Spokane, Washington, United States
Countries
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Other Identifiers
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SJRC-CS/PS
Identifier Type: -
Identifier Source: org_study_id
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