Signature Personalised Patient Care System With the Vanguard Knee System Study



Status:Recruiting
Conditions:Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:March 2010
End Date:May 2023
Contact:Maggie Shen
Email:maggie.shen@biomet.com

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Study on the Signature Personalised Patient Care System With the Vanguard Knee System

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.

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. Other outcomes will include knee assessments and patient questionnaires.

Inclusion Criteria:

- painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis,
traumatic arthritis where one or more of the knee compartments are involved

- correction of varus, valgus or posttraumatic deformity

- correction or revision of unsuccessful osteotomy (wedge cut from bone to improve
alignment), or arthrodesis (fusion)

- need to obtain pain relief and improve function

- ability and willingness to follow instructions, including control of weight and
activity level.

- a good nutritional state

- must have reached full skeletal maturity

- able and willing to undergo an MRI scan

Exclusion Criteria:

- infection

- sepsis

- osteomyelitis

- failure of a previous joint replacement
We found this trial at
2
sites
New York, New York 10065
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New York, NY
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Brisbane, Queensland 4131
Principal Investigator: Iulian Nusem
Phone: 07 32998235
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Brisbane,
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