I-beam and Cruciate Tibial Components Used in Total Knee Replacement

Biomet Orthopedics, LLC100 enrolled

Overview

The purpose of this study is to compare the clinical outcomes of using an I-beam or cruciate tibial component in total knee replacement.

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Degenerative Arthritis Osteoarthritis Rheumatoid Arthritis Knee Arthritis

Interventions

I-beam designDEVICE

This group will utilize tibial components with an I-beam design for total knee replacement.

Cruciate designDEVICE

This group will utilize tibial components with cruciate designs for total knee replacement.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartment are involved. * Patients requiring correction of varus, valgus, or posttraumatic deformity * Patients requiring correction of revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure. Exclusion Criteria: * Patients with infection, sepsis, or osteomyelitis.

Locations (1)

Biomet Orthopedics, LLC

Warsaw, Indiana, United States

Outcomes

Primary Outcomes

Revision rate

Time frame: 10 years

Data from ClinicalTrials.gov

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