Prospective Data Collection on Cementless Oxford Partial Knee

NCT ID: NCT00760188

Last Updated: 2017-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2011-12-31

Study Completion Date

2011-12-31

Brief Summary

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Prospective data collection on clinical and radiographic outcomes of Cementless oxford Partial Knee.

Detailed Description

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Prospective radiographic and clinical data collection on outcomes of Cementless oxford Partial Knee. Screened radiographs are taken postoperatively and after 12 months. Oxford Knee Scores, SF12 Health Questionnaires and American Knee Society Radiographic Assessment are taken at 12 month follow-up.

Conditions

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Arthroplasty, Replacement, Knee

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Cementless Oxford Partial Knee

Cementless Oxford Partial Knee Replacement

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients undergoing primary knee arthroplasty
2. Patients with one of the following primary diagnoses in the medial compartment of the knee:

* Osteoarthritis,
* Avascular necrosis

Exclusion Criteria

1. Inability to co-operate with and complete the study.
2. Inadequate fixation of cementless components. If either before or after randomization the surgeon feels that cementless fixation is inadequate, cemented components should be inserted.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Zimmer Biomet

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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N Hunt

Role: STUDY_DIRECTOR

Zimmer Biomet

Locations

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Rami Sorial , FRACS

Penrith, , Australia

Site Status

Countries

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Australia

Other Identifiers

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BMET AU 01

Identifier Type: -

Identifier Source: org_study_id

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