Total Knee Replacement With Duracon® and Vanguard™ Prostheses

Biomet Orthopedics, LLC150 enrolled

Overview

The purpose of this study is to compare range of motion, Knee Society Scores, and duration of surgery for different total knee prostheses.

Study Type

OBSERVATIONAL

Enrollment

150

Conditions

Degenerative Arthritis Osteoarthritis Rheumatoid Arthritis Knee Arthritis

Interventions

Duracon®DEVICE

This group utilizes the Duracon® prostheses for total knee replacement.

Vanguard™DEVICE

This group will utilize the Vanguard™ prostheses 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 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: * Patients with infection, sepsis, or osteomyelitis.

Locations (1)

Biomet Orthopedics, Inc.

Warsaw, Indiana, United States

Outcomes

Primary Outcomes

Range of motion, Knee Society Score, Duration of surgery

Time frame: 1 year

Data from ClinicalTrials.gov

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