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Prospective Data Collection on Cementless Oxford Partial Knee

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Zimmer Biomet

Status

Withdrawn

Conditions

Arthroplasty, Replacement, Knee

Treatments

Device: Cementless Oxford Partial Knee

Study type

Observational

Funder types

Industry

Identifiers

NCT00760188
BMET AU 01

Details and patient eligibility

About

Prospective data collection on clinical and radiographic outcomes of Cementless oxford Partial Knee.

Full description

Prospective radiographic and clinical data collection on outcomes of Cementless oxford Partial Knee. Screened radiographs are taken postoperatively and after 12 months. Oxford Knee Scores, SF12 Health Questionnaires and American Knee Society Radiographic Assessment are taken at 12 month follow-up.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients undergoing primary knee arthroplasty

  2. Patients with one of the following primary diagnoses in the medial compartment of the knee:

    • Osteoarthritis,
    • Avascular necrosis

Exclusion criteria

  1. Inability to co-operate with and complete the study.
  2. Inadequate fixation of cementless components. If either before or after randomization the surgeon feels that cementless fixation is inadequate, cemented components should be inserted.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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