About this trial

The goal of this observational study is to learn about functional and patient reported outcomes in patient undergoing total wrist replacement with the KinematX total wrist replacement study.

The main questions it aims to answer are:

* What is the range of motion (flexion, extension, radial, ulnar, grip and pinch strength) at 3-, 6-, and 12-months after surgery and yearly up to 10 years among patients having total wrist replacement with the KinematX implant. * What are the patient reported outcomes (PROMIS, PRWE, HSS wrist expectations) at 3-, 6-, and 12-months after surgery and yearly up to 10 years among patients having total wrist replacement with the KinematX implant. * How do range of motion and patient reported outcomes change over the 10 years after total wrist replacement surgery?

Participants will be followed according to standard of care and preoperative and post-operative information for up to 10 years after surgery will be collected and entered into an electronic data base. Patients are eligible to enroll into the registry before or after they have had their wrist replacement surgery.

Eligibility criteria

Qualifiers

osteoarthritis or post-traumatic arthritis

scapholunate advanced collapse (SLAC/SNAC wrist),

inflammatory arthritis (rheumatoid, psoriatic, other),

crystalline advanced collapse (SCAC),

Disqualifiers

<18 years of age

>85 years of age

Prisoners

Children

Trial design

Treatments tested in this trial

  • KinematX total wrist arthroplasty system

Treatment groups

50 Participants
are divided into 1 treatment group

Locations

4
Loma Linda University92354, Loma LindaCalifornia, United States
Florida Orthopaedic Institute33637, TampaFlorida, United States
Franciscan Health46237, IndianapolisIndiana, United States
Hospital for Special Surgery10021, New YorkNew York, United States

Sponsors and collaborators

Extremity Medical

Lead sponsor