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A Study to Evaluate the DePuy Minimally Invasive Unicompartmental Knee

NCT00734084 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 247

Last updated 2015-06-09

No results posted yet for this study

Summary

The primary purpose of this investigation is to evaluate the surgical performance of the DePuy Minimally Invasive (Preservation) Unicompartmental Knee and Instrumentation in a Multi-centre setting.

The secondary objective of this investigation is to evaluate the long-term survivorship of the DePuy Minimally Invasive (Preservation) Unicompartmental Knee.

Conditions

Interventions

DEVICE

Preservation Unicompartmental Knee

Minimally invasive orthopaedic implant for single compartment knee arthritis

Sponsors & Collaborators

  • DePuy International

    lead INDUSTRY

Principal Investigators

  • Kim Dwyer, Ph.D · DePuy Synthes Joint Reconstruction

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-06-30
Primary Completion
2004-12-31
Completion
2008-04-30

Countries

  • Australia

Study Locations

More Related Trials

Entities

Diseases

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 NCT00734084 on ClinicalTrials.gov