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Oxford Partial Knee Replacement. A Randomized Clinical Trial of Three Implant Types

NCT00679120 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2023-11-22

No results posted yet for this study

Summary

The purpose of this scientific study is to clarify whether there is a relationship between the appearance of radiolucent lines in bone-cement interphase of the tibial component of the different models of the Oxford Uni Knee prosthesis and poor prognosis of these prostheses. This will be accomplished in a se-ries of three different Oxford Uni Knees.

Conditions

  • Osteoarthritis, Knee

Interventions

DEVICE

Oxford Uni Knee

Oxford Uni Knee inserted at the time of surgery

DEVICE

Oxford Uni Knee

Oxford Uni Knee inserted at the time of surgery

DEVICE

Oxford Uni Knee

Oxford Uni Knee inserted at the time of surgery (porous coated and HA coated)

Sponsors & Collaborators

  • Aarhus University Hospital

    collaborator OTHER

  • Vejle Hospital

    collaborator OTHER

  • Zimmer Biomet

    collaborator INDUSTRY

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Kjeld Soballe, MD, Prof. · Orthopaedic Center, Aarhus University Hospital, Tage-Hansens Gade 2, 8000 Aarhus C, Denmark

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-05-31
Primary Completion
2017-10-31
Completion
2024-08-31

Countries

  • Denmark

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 NCT00679120 on ClinicalTrials.gov