CompletedNot Applicable

Ankle Joint Replacement Outcomes Study

United States76 participantsStarted 2007-10-31

Plain-language summary

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.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Exclusion Criteria: * 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

What they're measuring

Survivorship of Salto Talaris Ankle Implant

Timeframe: 10 years

Trial details

NCT IDNCT00503438

SponsorSmith & Nephew, Inc.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2023-04-21

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