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In Vivo Kinematics for Subjects Having a MicroPort Medial Pivot or DePuy Attune PCR TKA

NCT04103502 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2026-05-05

No results posted yet for this study

Summary

In vivo knee kinematics will be assessed for 20 subjects that have been implanted with either a MicroPort Medial Pivot or DePuy Attune posterior cruciate retaining (PCR) total knee arthroplasty (TKA) by Dr. Russell Nevins of Nevada Orthopedic \& Spine Center \[this is the location from which participants will be recruited\].

Conditions

  • Total Knee Arthroplasty
  • Osteo Arthritis Knee
  • Knee Injuries
  • Knee Imlant

Interventions

DEVICE

MicroPort Medial Pivot TKA

Subjects will have been implanted with the MicroPort Medial Pivot TKA

DEVICE

DePuy Attune PCR TKA

Subjects will have been implanted with the DePuy Attune PCR TKA

Sponsors & Collaborators

  • MicroPort Orthopedics Inc.

    collaborator INDUSTRY

  • The University of Tennessee, Knoxville

    lead OTHER

Principal Investigators

  • Richard Komistek, Ph.D. · The University of Tennessee

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-31
Primary Completion
2025-12-15
Completion
2025-12-15
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 NCT04103502 on ClinicalTrials.gov