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A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee
Sponsor: Zimmer Biomet
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
Conditions
Interventions
Vanguard SSK 360 with PS Bearing
non-constrained tibial bearing
Vanguard SSK 360 with PSC bearing
constrained tibial bearing
Vanguard DA 360
Dual-articulation device, only cleared in EU
Vanguard 360 TiNbN Femur with PS bearing
non-constrained tibial bearing, titanium niobium nitride coated Vanguard 360 femur
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