CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 100 enrolled
Drug / intervention
OtisMed® ShapeMatch® Technology +3 moredevice
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.

Search/NCT02527148
NCT02527148N/ACompleted

A Prospective, Randomized, Controlled Trial of Mechanical Axis vs Kinematic Alignment in TKR - With a Follow-up, Longitudinal Study of the Clinical and Radiographic Outcomes

Stryker South Pacific·interventional·Posted Aug 18, 2015·Updated May 15, 2025

In Brief

A clinical study evaluating OtisMed® ShapeMatch® Technology, Stryker Precision Knee Navigation, and 2 other interventions for Arthroplasties and Knee Replacement. Completed, enrolled 100 participants.

Detailed Summary

This is a prospective, randomized, longitudinal study of the clinical outcomes of osteoarthritis patients treated by two different alignment philosophies for total knee replacement. In this study ShapeMatch® cutting guides will be compared to the conventional approach.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
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Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedAug 18, 2015
Enrollment StartAug 4, 2011
Primary CompletionApr 9, 2018
Study CompletionDec 19, 2018
TodayJul 2, 2026
Enrollment to primary: 6.7 yearsPosted 10.9 years ago

Interventions

OtisMed® ShapeMatch® Technologydevice

The appropriate Stryker ShapeMatch® Cutting Guides will be used to guide the surgeons bone resections. The surgeon will implant the knee prostheses following the surgical protocol for Triathlon® Knee System with OtisMed® ShapeMatch® Technology

Stryker Precision Knee Navigationdevice

Stryker PrecisioN Knee (4.0) Navigation System, comprising of computer hardware and software and associated instrumentation, will be used for intra-operative alignment and orientation of implant. Navigation trackers will be secured to the femur and tibia and registration of the limb will be undertaken according to the PrecisioN Knee System surgical technique.Femoral and tibial resections, followed by device implantation, will be performed according to the Triathlon Knee System Surgical Protocol.

Total Knee Replacementprocedure

Stryker Triathlon® Total Knee Systemdevice

Prosthetic components to be implanted including * Triathlon® Cruciate Retaining (CR) Total Knee System (cemented), including Femoral Component and Primary Tibial Baseplate; * Triathlon® Cruciate Substituting (CS) X3® polyethylene insert; * Triathlon® X3 Patella (asymmetric) - treated selectively by surgeon.