Total Knee Arthroplasty Functional Outcomes Study Research Design

NCT02228538 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2023-10-25

No results posted yet for this study

Summary

The purpose of this study is to obtain patient oriented and clinically oriented physical function outcomes both pre-operatively and post-operatively in patients receiving a total knee arthroplasty.

Conditions

  • Osteoarthritis of the Knee

Interventions

DEVICE

Total knee arthroplasty patients

ConforMIS iTotal (CR) knee implant system \& off-the-shelf standard knee implant system from various manufacturers

Sponsors & Collaborators

  • Ochsner Health System

    collaborator OTHER
  • Restor3D

    lead INDUSTRY

Principal Investigators

  • Deryk Jones, MD · Ochsner Heath System

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-10-31
Primary Completion
2015-05-31
Completion
2016-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02228538 on ClinicalTrials.gov