Triathlon Tritanium Cone Augments Outcomes Study
NCT: NCT02521103 · ACTIVE_NOT_RECRUITING
NCT IDNCT02521103
StatusACTIVE_NOT_RECRUITING
Start Date2015-08
Completion2028-03-31
SponsorStryker Orthopaedics (INDUSTRY)
First posted
Last updated
Brief Summary
The purpose of this study was to evaluate the success rate of the Triathlon Tritanium Cone Augment with the Triathlon TS Total Knee System at 2 years postoperative, defined as absence of revision of the Femoral Cone Augment or Tibial Cone augment for aseptic loosening.
Frequently Asked Questions
What is Triathlon Tritanium Cone Augments Outcomes Study?
Triathlon Tritanium Cone Augments Outcomes Study is a clinical trial registered under NCT02521103. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT02521103?
The current status of NCT02521103 (Triathlon Tritanium Cone Augments Outcomes Study) is: ACTIVE_NOT_RECRUITING.
When did Triathlon Tritanium Cone Augments Outcomes Study start?
Triathlon Tritanium Cone Augments Outcomes Study started on 2015-08.
Related Devices
K172326Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee SystemStryker Orthopaedics
K173849Triathlon Total Knee SystemStryker Orthopaedics
K242831Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee SystemHowmedica Osteonics Corp., Dba Stryker Orthopaedics
K153345Stryker Orthopaedics Hip Systems Labeling UpdateStryker Orthopaedics
K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker Orthopaedics
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.