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To Determine the Gait and Functional Improvement in Total Knee Arthroplasty

NCT04057885 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2020-02-26

No results posted yet for this study

Summary

This is an observational study to understand the effects of soft-tissue balancing on gait, function and rehabilitation potential after sensor-assisted Total Knee Arthroplasty

Conditions

  • Degenerative Arthritis

Interventions

DEVICE

Orthosensor™ VERASENSE™ Knee System

A group of patients will receive a total knee arthroplasty using the Orthosensor device

Sponsors & Collaborators

  • Orthosensor, Inc.

    collaborator INDUSTRY

  • LifeBridge Health

    lead OTHER

Principal Investigators

  • Michael A. Mont, M.D. · Director, Rubin Institute for Advanced Orthopedics and Joint Preservation

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2017-05-15
Primary Completion
2018-07-31
Completion
2018-07-31
FDA Device
Yes

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 NCT04057885 on ClinicalTrials.gov