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Outcome Analysis of the Oxford Partial Knee Arthroplasty

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00759616
First Posted: September 25, 2008
Last Update Posted: June 16, 2017
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.
Collaborator:
Dartmouth General Hospital
Information provided by (Responsible Party):
Zimmer Biomet
  Purpose
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.
  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


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

Inclusion Criteria:

  • Patient Suitable for Knee Replacement

Exclusion Criteria:

  Contacts and Locations
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


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

Responsible Party: Zimmer Biomet
ClinicalTrials.gov Identifier: NCT00759616     History of Changes
Other Study ID Numbers: BMET CA 03
First Submitted: September 24, 2008
First Posted: September 25, 2008
Last Update Posted: June 16, 2017
Last Verified: June 2017

Keywords provided by Zimmer Biomet:
Knee Replacement