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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
125 participants
OBSERVATIONAL
2007-12-31
2016-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Cruciate Substituting Tibial Insert
Stryker Triathlon® CS Tibial Insert
Posterior Stabilized Tibial Insert
Stryker Triathlon® PS Tibial Insert
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Stryker Triathlon® CS Tibial Insert
Stryker Triathlon® PS Tibial Insert
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
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
Meet the organizations funding or collaborating on the study and learn about their roles.
Spokane Joint Replacement Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
David F. Scott, MD
PI
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
David F Scott, MD
Role: PRINCIPAL_INVESTIGATOR
Spokane Joint Replacement Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Spokane Joint Replacement Center
Spokane, Washington, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
SJRC-CS/PS
Identifier Type: -
Identifier Source: org_study_id