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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02747836
Other study ID # 06-002950
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 2006
Est. completion date February 2025

Study information

Verified date April 2024
Source Mayo Clinic
Contact Lindsey Hobbs
Phone 507-293-9765
Email hobbs.lindsey@mayo.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the ability of ultrasound to measure the movement of tendons and nerves within the human carpal tunnel.


Description:

The overall goal of this project is to develop a novel ultrasonographic method to characterize the subsynovial connective tissue (SSCT) and detect differences between SSCT, median nerve and tendon motion for the evaluation and diagnosis of patients suspected of having carpal tunnel syndrome (CTS). CTS is usually diagnosed late in its evolution, by measuring electrophysiological changes in median nerve function. Once these changes have occurred, surgery is often the only effective treatment. At an earlier stage of evolution, non-surgical treatment might be more effective. Although ultrasonography and magnetic resonance imaging (MRI) have recently been used to measure changes in median nerve shape in CTS, such approaches also only capture late changes. Thus, a method for detection of CTS that could identify pathology before function or structure of the nerve is compromised could prevent significant morbidity and transition to a permanent neuropathy. One promising opportunity is presented in the subsynovial connective tissue (SSCT), which surrounds the tendons in the carpal tunnel. One of the most characteristic findings in surgically treated patients with CTS is a non-inflammatory fibrosis of the SSCT. Some investigators have suggested that the SSCT may be the cause of the nerve compression in CTS. In our previous work, the investigators have demonstrated differences in the mechanical properties, motion and thickness of the SSCT in patients with CTS compared to normals. More recently, an animal model has been described in which the structural changes in the SSCT have been shown to precede the changes in nerve function. The investigators have demonstrated in cadaver studies that the normal SSCT can be imaged by ultrasound, and its motion, velocity, and thickness distinguished from that of the nearby tendon and nerve. Here the investigators propose to leverage this work, and study the ability of ultrasound to detect SSCT thickness and motion in individuals with and without CTS. Based on our preliminary research, the investigators formulate the following central hypothesis: An increase in SSCT thickness and changes in sliding velocities of the SSCT with respect to the corresponding tendon are indicative of CTS. In addition, this material property change at SSCT affects median nerve motions and transformations. This is because the SSCT becomes fibrotic in CTS, and the fibrosis alters the normal SSCT-median nerve-tendon functional relationship.


Recruitment information / eligibility

Status Recruiting
Enrollment 360
Est. completion date February 2025
Est. primary completion date February 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Patients will be selected from among those undergoing diagnostic work up for CTS in the pre-treatment period. CTS diagnosis will be confirmed clinically and by nerve conduction study Exclusion Criteria: - The following disorders will be criteria for exclusion: - any history of cervical radiculopathy - rheumatoid arthritis - osteoarthritis - degenerative joint disease - flexor tendinitis - gout hemodialysis - sarcoidosis - peripheral nerve disease - amyloidosis - traumatic injuries to the ipsilateral arm

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ultrasound of the wrist
using sound waves to create images capturing the movement of the SSCT and flexor tendon and transformation of the median nerve in the wrist

Locations

Country Name City State
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Study the ability of ultrasound to detect differences in SSCT thickness in individuals with and without CTS. Measure and evaluate SSCT thickness at the time of study enrollment. patients are enrolled only for the purpose of obtaining a single imaging study.
Secondary study the ability to detect differences in median nerve and tendon motion in the transverse plane of individuals with and without carpal tunnel syndrome measure displacement of tendons and nerves and the carpal tunnel in the dorsal-palmar and radioulnar directions at time of enrollment. patients are enrolled only for the purpose of obtaining a single imaging study.
Secondary Study the ability of ultrasound to detect differences in SSCT motion in individuals with and without CTS. Measure and evaluate changes in sliding velocities of the SSCT with respect to the corresponding tendon at the time of study enrollment. patients are enrolled only for the purpose of obtaining a single imaging study.
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