Total Knee Replacement Using Simplex® or Cobalt™ Bone Cement

Zimmer Biomet

Overview

The purpose of this study is to collect radiographic and clinical outcomes of total knee replacement using Simplex® or Cobalt™ Bone Cement.

Study Type

OBSERVATIONAL

Conditions

Osteoarthritis Rheumatoid Arthritis Traumatic Arthritis Knee Arthritis

Interventions

Simplex® Bone CementDEVICE

This arm will utilize Simplex® Bone Cement in total knee replacement.

Cobalt™ Bone CementDEVICE

This arm utilizes Cobalt™ Bone Cement in 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 compartments are involved * Patients requiring correction of varus, valgus, or posttraumatic deformity * Patients requiring correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure Exclusion Criteria: * Infection, sepsis, and osteomyelitis

Locations (1)

Biomet Orthopedics, LLC

Warsaw, Indiana, United States

Outcomes

Primary Outcomes

Radiographic analysis and Knee Society Score

Time frame: 10 years

Data from ClinicalTrials.gov

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