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Outcome Analysis of the Oxford Partial Knee Arthroplasty

This study has been completed.
Dartmouth General Hospital
Information provided by (Responsible Party):
Zimmer Biomet Identifier:
First received: September 24, 2008
Last updated: June 15, 2017
Last verified: June 2017
Prospectively monitor the patients receiving the Oxford Partial knee arthroplasty

Condition Intervention
Knee Arthroplasty Device: Oxford Partial Knee

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Outcome Analysis of the Oxford Partial Knee Arthroplasty

Resource links provided by NLM:

Further study details as provided by Zimmer Biomet:

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

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

Enrollment: 156
Study Start Date: April 2003
Study Completion Date: June 2009
Primary Completion Date: June 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: 1 Device: Oxford Partial Knee
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.

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:

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00759616

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

Responsible Party: Zimmer Biomet Identifier: NCT00759616     History of Changes
Other Study ID Numbers: BMET CA 03
Study First Received: September 24, 2008
Last Updated: June 15, 2017

Keywords provided by Zimmer Biomet:
Knee Replacement processed this record on September 21, 2017