Status:

COMPLETED

Costs and Benefits of ConforMIS iTotal® Knee Replacement System Versus Standard Total Knee

Lead Sponsor:

Restor3D

Conditions:

Osteoarthritis,Knee

Eligibility:

All Genders

19+ years

Brief Summary

The purpose of this study is to evaluate the costs and benefits of the ConforMIS iTotal® total knee replacement system versus standard total knee arthroplasty. This study is designed to illustrate th...

Detailed Description

STUDY DESIGN The study is a two-arm single-center, consecutively enrolled retrospective study. Patients enrolled will have previously received either an iTotal CR knee replacement or a standard total ...

Eligibility Criteria

Inclusion

  • Patient has received an iTotal or a standard total knee replacement
  • Willingness to participate in the clinical study and to give informed consent, if necessary, as determined during IRB review
  • \>18 years of age

Exclusion

  • Participation in another clinical study that could confound results
  • Patient is less than 3 months post-op

Key Trial Info

Start Date :

July 1 2013

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 1 2014

Estimated Enrollment :

235 Patients enrolled

Trial Details

Trial ID

NCT01899417

Start Date

July 1 2013

End Date

March 1 2014

Last Update

October 25 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

JFK Medical Center

Atlantis, Florida, United States, 33462

Costs and Benefits of ConforMIS iTotal® Knee Replacement System Versus Standard Total Knee | DecenTrialz