Outcome Analysis of the Oxford Partial Knee Arthroplasty

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00759616

Enrollment

156

Registered

2008-09-25

Start date

2003-04-30

Completion date

2009-06-30

Last updated

2017-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Arthroplasty

Keywords

Knee Replacement

Brief summary

Prospectively monitor the patients receiving the Oxford Partial knee arthroplasty

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.

Interventions

DEVICEOxford Partial Knee

Oxford Partial Knee

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* Patient Suitable for Knee Replacement

Design outcomes

Primary

Measure	Time frame
WOMAC, SF12, oxford Knee,KSCRS	3weeks, 3months,6months, yearly

Secondary

Measure	Time frame
Length of Hospital Stay	Postop

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026