Prospective Data Collection on Cementless Oxford Partial Knee
Information source: Biomet, Inc.
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Arthroplasty, Replacement, Knee
Intervention: Cementless Oxford Partial Knee (Device)
Phase: N/A
Status: Recruiting
Sponsored by: Biomet, Inc.
Summary
Prospective data collection on clinical and radiographic outcomes of Cementless oxford
Partial Knee.
Clinical Details
Official title: Prospective Clinical Evaluation of the Cementless Oxford Partial Knee
Study design: Cohort, Prospective
Primary outcome: American Knee Society Score
Secondary outcome: Radiographic AssessmentOxford Knee Score, SF12
Detailed 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.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
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.
Locations and Contacts
Rami Sorial , FRACS, Penrith, Australia; Recruiting R Sorial, FRACS, Phone: 02.4721.2217
Additional Information
Starting date: July 2004
Ending date: September 2012
Last updated: October 2, 2008
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