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A Clinical Investigation of the Vanguard™ Complete Knee System

NCT00698854 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 552

Last updated 2024-09-19

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 Vanguard™ Complete Knee System.

Conditions

Interventions

DEVICE

Vanguard™ Complete Knee System

Primary Total Knee System, Cruciate-Retaining (CR) or Posterior-Stabilized (PS)

DEVICE

Vanguard™ Patient-Specific Femur

Primary Total Knee System used with Signature technique to provide a patient-specific femur

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Kacy C Arnold, RN MBA · Zimmer Biomet

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-03-31
Primary Completion
2021-01-31
Completion
2024-03-31

Countries

  • United States

Study Locations

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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 NCT00698854 on ClinicalTrials.gov