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Gait and Functional Outcomes Study Following Total Knee Arthroplasty With Medial-pivot or Posterior-stabilized Implants

NCT02589197 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2022-11-25

No results posted yet for this study

Summary

MicroPort Orthopedics (MPO) is conducting this study to build upon the results of a previous study which showed the Medial Pivot (MP) system required lower quadriceps activation than subjects implanted with a Posterior stabilized (PS) system preforming the same activities of daily living.

Conditions

  • Joint Disease

Interventions

DEVICE

Group 1 (Medial-Pivot)

EVOLUTION® Total Knee Arthroplasty Medial Pivot system with CS inserts

DEVICE

Group 2 (Posterior-Stabilized)

Zimmer® NexGen® Total Knee Arthroplasty system with PS inserts

Sponsors & Collaborators

  • University of Ottawa

    collaborator OTHER

  • The Ottawa Hospital

    collaborator OTHER

  • MicroPort Orthopedics Inc.

    lead INDUSTRY

Principal Investigators

  • Geoffrey Dervin, MD · Ottawa Hospital

Eligibility

Min Age
45 Years
Max Age
76 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-07-13
Primary Completion
2022-09-30
Completion
2022-09-30

Countries

  • Canada

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 NCT02589197 on ClinicalTrials.gov