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Signature Personalised Patient Care System With the Vanguard Knee System Study

NCT01092312 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 325

Last updated 2017-09-05

No results posted yet for this study

Summary

The purpose of this study is to determine whether the percentage cases which have ideal mechanical axial alignment using the Vanguard total Knee implant with the Signature cutting blocks is higher than those without the use of Signature when measured immediately post-operatively.

Conditions

  • Arthroplasty, Replacement, Knee

Interventions

PROCEDURE

Vanguard Knee System with Signature Knee Guide

Use of Signature Knee Guide

PROCEDURE

Vanguard Knee System with conventional Instruments

Vanguard Knee System with conventional Instruments

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Gordon Morrison, MBChB · The Queen Elizabeth Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2016-09-30
Completion
2016-09-30

Countries

  • United States
  • Australia
  • Austria
  • Belgium
  • Denmark
  • France
  • Netherlands
  • Portugal
  • Sweden
  • United Kingdom

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 NCT01092312 on ClinicalTrials.gov