At a glance
ClinicalIndex Comparison RecordN/ACompleted· 409 enrolled
Drug / intervention
Triathlon® PS Total Knee Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Prospective, Post-market, Multi-center Study of the Outcomes of the Triathlon® Posteriorly Stabilized (PS) Total Knee System
In Brief
A clinical study evaluating Triathlon® PS Total Knee System for Arthroplasty, Replacement, Knee. Completed, enrolled 409 participants across 11 sites.
Detailed Summary
The purpose of this study is to evaluate the clinical outcomes (range of motion, pain, function, radiographic stability, and health related quality of life) of patients receiving the Triathlon® Posterior Stabilized (PS) Total Knee System. These outcomes will be evaluated using pre-operative scores and comparing them to post-operative scores in addition to being compared with cases who received the Scorpio® PS implant.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsArthroplasty, Replacement, Knee
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartDec 2005
First PostedAug 2009
Primary CompletionMar 2011
Study CompletionJan 2014
TodayJul 2026
First PostedAug 12, 2009
Enrollment StartDec 1, 2005
Primary CompletionMar 1, 2011
Study CompletionJan 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5.3 yearsPosted 16.9 years ago
Interventions
Triathlon® PS Total Knee Systemdevice
Triathlon® PS Total Knee system