Total Knee Replacement With Duracon® and Vanguard™ Prostheses

Zimmer Biomet

Status: Terminated

Conditions: Knee Arthritis; Osteoarthritis; Degenerative Arthritis; Rheumatoid Arthritis

Treatments: Device: Duracon®; Device: Vanguard™

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00588887

105-U-014

Details and patient eligibility

About

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

Enrollment: 150 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

150 participants in 2 patient groups

1

Treatment:

Device: Duracon®

2

Treatment:

Device: Vanguard™