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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:
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.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
one of the following diagnoses and planned (or previously completed) total wrist arthroplasty with the KinematX total wrist:
Exclusion criteria
<18 years of age
>85 years of age
Prisoners
Children
Pregnant women
Contraindications to receiving the KinematX:
50 participants in 1 patient group
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Central trial contact
Brian Smekal
Data sourced from clinicaltrials.gov
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