Post-Market Study of the 3DKnee™ System

NCT00819481 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 229

Last updated 2021-03-16

No results posted yet for this study

Summary

The purpose of this study is to evaluate the use and efficacy of the 3DKnee™ System for total knee replacement surgery.

Conditions

Interventions

DEVICE

3DKnee™ System

Total knee replacement joint for subjects with knee osteoarthritis and willing to participate in the study.

Sponsors & Collaborators

  • Encore Medical, L.P.

    lead INDUSTRY

Principal Investigators

  • John W. McAllister, M.D. · St. Peter's Bone and Joint Surgery

  • Barry J Waldman, M.D. · OrthoMaryland

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2014-01-31
Completion
2018-10-31

Countries

  • United States

Study Locations

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Entities

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 NCT00819481 on ClinicalTrials.gov