RECRUITING

A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee

Description

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.

Conditions

OsteoarthritisRheumatoid ArthritisTraumatic ArthritisPost Traumatic DeformityComplications; ArthroplastyDeformity of Limb
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Related Conditions:

OsteoarthritisRheumatoid ArthritisTraumatic ArthritisPost Traumatic DeformityComplications; ArthroplastyDeformity of Limb

Study Overview

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Study Details

Study overview

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.

A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee

A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee

Condition
Osteoarthritis
Intervention / Treatment

-

Contacts and Locations

Morton Grove

Illinois Bone and Joint, Morton Grove, Illinois, United States, 60053

Henderson

Orthopedic Institute of Henderson, Henderson, Nevada, United States, 89052

Salt Lake City

University of Utah Orthopedic Center, Salt Lake City, Utah, United States, 84108

Richmond

OrthoVirginia West End Orthopedic Clinic, Richmond, Virginia, United States, 23235

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved.
  • * Correction of varus, valgus or post-traumatic deformity
  • * Correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure
  • * Ability and willingness of the patient to attend follow-up visit.
  • * Willing to give written informed consent
  • * Patients are at least 18 years of age, no upper age limit, must have reached full skeletal maturity.
  • * infection
  • * sepsis
  • * osteomyelitis
  • * An uncooperative patient or a patient with neurologic disorders who is incapable of following directions
  • * Osteoporosis
  • * Metabolic disorders which may impair brain function
  • * Osteomalacia
  • * Distant foci of infections which may spread to the implant site
  • * Rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram
  • * Vascular insufficiency, muscular atrophy, neuromuscular disease
  • * Incomplete or deficient soft tissue surrounding the knee

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Zimmer Biomet,

Hassan Achakri, PhD, STUDY_DIRECTOR, Zimmer Biomet

Study Record Dates

2031-12