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Kinematics in Posterior Cruciate Retaining and Bi-Cruciate Retaining Total Knee Replacements

NCT03088748 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2021-10-12

Study results available
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Summary

The purpose of the study is to acquire kinematic in vivo fluoroscopy data from subjects who were implanted with the Smith \& Nephew Journey II posterior cruciate retaining (PCR) total knee arthroplasty (TKA) or Journey II bi-cruciate retaining (BCR) TKA. CMR has previously collected data for the Smith \& Nephew BCS TKA and compared these kinematics data to those of normal knees.

Conditions

  • Arthroplasty, Replacement, Knee
  • Osteoarthritis, Knee

Interventions

DEVICE

Journey II posterior cruciate retaining total knee arthroplasty

DEVICE

Journey II posterior bi-cruciate retaining total knee arthroplasty

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    collaborator INDUSTRY

  • The University of Tennessee, Knoxville

    lead OTHER

Principal Investigators

  • Richard Komistek · The University of Tennessee

Eligibility

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

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2020-11-09
Completion
2020-11-09
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 NCT03088748 on ClinicalTrials.gov