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Outcome Analysis of the Oxford Partial Knee Arthroplasty

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00759616
Recruitment Status : Completed
First Posted : September 25, 2008
Last Update Posted : June 16, 2017
Dartmouth General Hospital
Information provided by (Responsible Party):
Zimmer Biomet

Brief Summary:
Prospectively monitor the patients receiving the Oxford Partial knee arthroplasty

Condition or disease Intervention/treatment
Knee Arthroplasty Device: Oxford Partial Knee

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.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 156 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Outcome Analysis of the Oxford Partial Knee Arthroplasty
Study Start Date : April 2003
Primary Completion Date : June 2009
Study Completion Date : June 2009

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Knee Replacement
U.S. FDA Resources

Arm Intervention/treatment
Experimental: 1 Device: Oxford Partial Knee
Oxford Partial Knee

Primary Outcome Measures :
  1. WOMAC, SF12, oxford Knee,KSCRS [ Time Frame: 3weeks, 3months,6months, yearly ]

Secondary Outcome Measures :
  1. Length of Hospital Stay [ Time Frame: Postop ]

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Patient Suitable for Knee Replacement

Exclusion Criteria:

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00759616

Dartmouth General Hospital
Dartmouth, Canada
Sponsors and Collaborators
Zimmer Biomet
Dartmouth General Hospital

Responsible Party: Zimmer Biomet
ClinicalTrials.gov Identifier: NCT00759616     History of Changes
Other Study ID Numbers: BMET CA 03
First Posted: September 25, 2008    Key Record Dates
Last Update Posted: June 16, 2017
Last Verified: June 2017

Keywords provided by Zimmer Biomet:
Knee Replacement