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Evaluate the Safety, Functionality, and the Quality of Life of Patients Who Receive the Freedom Total Knee ® System

NCT02056470 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 211

Last updated 2020-03-30

No results posted yet for this study

Summary

Assess the safety and functionality of the Freedom Knee® system through a multi-center clinical trial. Study endpoints include a comparison of Pre-Surgery versus Post-Surgery data for:

1. Range of Motion
2. Quality of Life measurements using Knee Society Scale (KSS)
3. Survivorship as defined by 'No Revision' of baseline implant
4. Quality of Life measurements using the WOMAC Score

Conditions

  • Knee Joint Pain

Interventions

DEVICE

Freedom Total Knee

The Freedom Total Knee System is being implanted in subjects suitable for a total knee replacement

DEVICE

Total Knee Replacement

total Knee replacement implant

DEVICE

Freedom Total Knee System

Total Knee replacement implant

Sponsors & Collaborators

  • Maxx Orthopedics Inc

    lead INDUSTRY

Principal Investigators

  • Robert W Eberle · Director, Clinical Affairs

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2020-02-29
Completion
2020-03-31

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 NCT02056470 on ClinicalTrials.gov