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Outcome Analysis of the Oxford Partial Knee Arthroplasty

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Zimmer Biomet

Status

Completed

Conditions

Knee Arthroplasty

Treatments

Device: Oxford Partial Knee

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00759616
BMET CA 03

Details and patient eligibility

About

Prospectively monitor the patients receiving the Oxford Partial knee arthroplasty

Full 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.

Enrollment

156 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patient Suitable for Knee Replacement

Exclusion Criteria:

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

156 participants in 1 patient group

1
Experimental group
Treatment:
Device: Oxford Partial Knee

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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