Outcome Analysis of the Oxford Partial Knee Arthroplasty
Information source: Biomet, Inc.
Information obtained from ClinicalTrials.gov on November 03, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Knee Arthroplasty
Intervention: Oxford Partial Knee (Device)
Phase: N/A
Status: Recruiting
Sponsored by: Biomet, Inc.
Summary
Prospectively monitor the patients receiving the Oxford Partial knee arthroplasty
Clinical Details
Official title: Outcome Analysis of the Oxford Partial Knee Arthroplasty
Study design: Treatment, Open Label, Single Group Assignment, Safety/Efficacy Study
Primary outcome: WOMAC, SF12, oxford Knee,KSCRS
Secondary outcome: Length of Hospital Stay
Detailed description:
Utilization of systematic outcome measurements and specific designated time frames to monitor
patient satisfactions will assist in analysing this type of prosthesis and the post operative
period. Data collected will be added to the compiled information from previous studies in
relation to the Oxford knee.
Eligibility
Minimum age: N/A.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patient Suitable for Knee Replacement
Exclusion Criteria:
Locations and Contacts
Dartmouth General Hospital, Dartmouth, Canada; Recruiting
Vikram Venugopal, MD, Phone: (902) 469- 9667
Additional Information
Starting date: April 2003
Ending date: April 2010
Last updated: September 24, 2008
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