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ACTIVE NOT RECRUITING
NCT01542580

A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee

Sponsor: Zimmer Biomet

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate performance of the Vanguard 360 revision knee system utilizing offset on either the tibial component, femoral component, or both in terms of the restoration of mechanical alignment, clinical outcomes and survivorship.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

255

Start Date

2012-03

Completion Date

2031-12

Last Updated

2025-11-25

Healthy Volunteers

No

Interventions

DEVICE

Vanguard SSK 360 with PS Bearing

non-constrained tibial bearing

DEVICE

Vanguard SSK 360 with PSC bearing

constrained tibial bearing

DEVICE

Vanguard DA 360

Dual-articulation device, only cleared in EU

DEVICE

Vanguard 360 TiNbN Femur with PS bearing

non-constrained tibial bearing, titanium niobium nitride coated Vanguard 360 femur

DEVICE

Vanguard 360 TiNbN Femur with PSC bearing

constrained tibial bearing, titanium niobium nitride coated Vanguard 360 femur

Locations (12)

Illinois Bone and Joint

Morton Grove, Illinois, United States

Orthopedic Institute of Henderson

Henderson, Nevada, United States

University of Utah Orthopedic Center

Salt Lake City, Utah, United States

OrthoVirginia West End Orthopedic Clinic

Richmond, Virginia, United States

University Hopital Pellenberg

Pellenberg, Belgium

Aarhus university hospital

Aarhus, Denmark

Ch Lyon Sud

Lyon, France

Klinik fur Endoprothetik und gelenkchirurgie

Bad Wildbad, Germany

IRCCS Istituto Ortopedico Galeazzi

Milan, Italy

Azienda Ospedaliero Universitaria Pisana

Pisa, Italy

University Hospital Mutua de Terrasa

Terrassa, Spain

Royal Orthopaedic Hospital

Birmingham, United Kingdom