Assessment of Carpal Tunnel Syndrome by Shearwave Elastography

Status Enrolling by invitation

Clinical Trial Summary

This study is being done to test a new ultrasound method to detect possible stiffness problems within wrist(s). The purpose of this research is to the test the effectiveness of a new ultrasound method to check the nerve and surrounding tissue in both wrist of patient volunteers before and after treatment.

Clinical Trial Description

The ultrasound system is FDA approved. The risks associated with this research study are not beyond the normal risk of conventional ultrasound and should not cause you any discomfort. Ultrasound at the intensity levels and duration used in this study has not been shown to present risk to humans. The investigators will conduct the SWE study on the set time point when the patient returns for follow-up after the therapy (surgical decompression or corticosteroid injection). A set of pictures will be taken of patients wrists by the FDA approved ultrasound system. This system uses a special type of ultrasound for imaging your wrists. The ultrasound study will be repeated after 3 and 6 months after the treatments. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04804293
Study type	Interventional
Source	Mayo Clinic
Contact
Status	Enrolling by invitation
Phase	N/A
Start date	March 15, 2021
Completion date	December 20, 2026

View Details

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