Total Knee Replacement With Duracon® and Vanguard™ Prostheses

Terminated

• Conditions: Knee Arthritis; Osteoarthritis; Degenerative Arthritis; Rheumatoid Arthritis
• Interventions: Device: Vanguard™; Device: Duracon®

• Registration Number: NCT00588887
• Lead Sponsor: Biomet Orthopedics, LLC

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2005-06
• Study First Submitted: 2007-12-21
• Study First Submitted QC: 2008-01-03
• Study First Posted: 2008-01-09
• Primary Completion: 2008-02
• Study Completion: 2008-06
• Status Verified: 2017-06
• Last Update Submitted: 2017-06-19
• Last Update Posted: 2017-06-21

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 150

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.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
2	Vanguard™	-
1	Duracon®	-

Primary Outcome Measures

Name	Time	Method
Range of motion, Knee Society Score, Duration of surgery	1 year

Trial Locations

Locations (1)

Biomet Orthopedics, Inc.; 🇺🇸 Warsaw, Indiana, United States