Total Knee Replacement Using Simplex® or Cobalt™ Bone Cement

Zimmer Biomet

Status: Withdrawn

Conditions: Knee Arthritis; Traumatic Arthritis; Osteoarthritis; Rheumatoid Arthritis

Treatments: Device: Simplex® Bone Cement; Device: Cobalt™ Bone Cement

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00589485

102-U-012

Details and patient eligibility

About

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

Full description

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

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

• Infection, sepsis, and osteomyelitis

Trial design

0 participants in 2 patient groups

1

Treatment:

Device: Simplex® Bone Cement

2

Treatment:

Device: Cobalt™ Bone Cement