The KinematX Midcarpal Total Wrist Arthroplasty Registry

Summary

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

• Scapholunate Advanced Collapse (SLAC)
• Scapholunate Crystalline Advanced Collapse (SCAC)
• Scaphoid, Trapezium, and Trapezoid Advanced Collapse (STTAC)
• Carpal Tunnel Syndrome (CTS)
• Kienbock's Disease of Adults
• Radial Malunion
• Ulnar Translocation
• Post Traumatic Arthritis
• Inflammatory Arthritis
• Osteoarthritis
• Scaphoid Non-union Advanced Collapse (SNAC)

Eligibility basics and study details

Study type

Observational

Phase

Not applicable

Ages

18 to 85 years

Sex

All

Healthy volunteers

Not accepted

Sponsor

Extremity Medical

Last updated on ClinicalTrials.gov

November 15, 2023

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites