Ankle Joint Replacement Outcomes Study

Completed

Conditions studied: Osteoarthritis, Rheumatoid Arthritis, Post-Traumatic Arthritis, Septic Arthritis, Prior Ankle Fusion

In brief

This post market outcome study will look at the therapeutic results of the Salto Talaris Anatomic ankle prosthesis. The study population will consist of patients who will undergo an ankle arthroplasty procedure with a Salto Talaris ankle implant. An analysis will be conducted of the results, complications and revisions of this prosthesis based on the etiology for which the ankle arthroplasty was performed.

Key facts

Study ID

NCT00503438

Run by

Smith & Nephew, Inc.

People needed

76

Starts

2007-10-31

Expected to finish

2023-04-21

Last updated by the study team

2024-01-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects that need an ankle joint replacement due to arthritis or failed prior fusion.
• Subjects who have failed standard conservative management of their ankle condition

You may not qualify if…

• Class IV or higher anesthetic risk
• Subjects who are not able to comply with the study procedures
• Known contraindications to joint replacement such as active infection, complete talar necrosis, insufficient quality of bone stock, ligament laxity, severe osteopenia, Charcot's arthropathy
• Unwilling to be followed for 5 years

Where it is running

• Foot and Ankle Center of South Texas — San Antonio, Texas, United States
• Medical College of Wisconsin — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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