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Impact of Component Design and Fixation in Total Knee Arthroplasty

NCT03272178 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2021-12-01

No results posted yet for this study

Summary

The purpose of this study is to determine implant design and determine if method of fixation cemented versus cementless results in different bone loss patterns. The investigators also want to determine if clinical outcomes correlate with bone density changes.

Conditions

  • Arthroplasties, Knee Replacement

Interventions

DEVICE

Depuy total knee implant

patients from Dr Nunley's clinic will get a Depuy implant

DEVICE

Triathlon total knee implant

patients from Dr Barrack's clinic will get a Triathlon implant

Sponsors & Collaborators

  • Stryker Nordic

    collaborator INDUSTRY

  • Washington University School of Medicine

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-20
Primary Completion
2021-11-15
Completion
2021-11-15
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 NCT03272178 on ClinicalTrials.gov