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Oxford Partial Knee Comparative Instrument Pilot Study

NCT01410786 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2017-08-02

No results posted yet for this study

Summary

The purpose of this prospective clinical data-collection is to document the performance and clinical outcomes of the Oxford Partial Knee System using Signature Custom Guides and Conventional Instrumentation.

Conditions

  • Osteoarthritis, Knee

Interventions

PROCEDURE

Conventional Instrumentation

Standard Oxford surgical instruments

PROCEDURE

Signature Custom Guides

Signature Custom Guides used with Instruments in surgical technique

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Rod Maxwell · Canterbury Orthopaedic Services

Study Design

Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2015-05-31
Completion
2015-12-31

Countries

  • New Zealand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01410786 on ClinicalTrials.gov