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Association of Clinical Severity With Ultrasonographic, Electrophysiological, and Functional Parameters in Patients With Carpal Tunnel Syndrome: A Cross-Sectional Observational Study

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Carpal tunnel syndrome is one of the most common conditions caused by compression of a nerve at the wrist. It can lead to numbness, tingling, pain, weakness, and difficulty performing daily activities. Although nerve conduction studies are widely used to confirm the diagnosis and assess disease severity, ultrasonography has become an increasingly important, non-invasive diagnostic tool. However, the relationship between ultrasound findings, nerve conduction study results, hand function, and symptom severity has not been fully clarified. The purpose of this study is to investigate the relationship between the clinical severity of carpal tunnel syndrome and ultrasonographic, electrophysiological, and functional parameters. Participants with carpal tunnel syndrome will undergo ultrasonographic measurement of the median nerve, nerve conduction studies, hand grip strength assessment, pressure pain threshold measurement, and completion of the Boston Carpal Tunnel Questionnaire. The investigators hypothesize that greater clinical severity will be associated with larger median nerve cross-sectional area, more severe electrophysiological abnormalities, reduced hand grip strength, lower pressure pain threshold, and poorer functional status. The findings of this study may improve the understanding of the relationship between structural, electrophysiological, and functional changes in carpal tunnel syndrome and contribute to clinical evaluation and patient management.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
View:

• Adults aged 18 years or older

• Clinical findings consistent with carpal tunnel syndrome

• Carpal tunnel syndrome confirmed by electroneuromyography

• Ability to understand and complete the study assessments

• Provision of written informed consent

Locations
Other Locations
Turkey
Kanuni Sultan Suleyman Education and Research Hospital
RECRUITING
Küçükçekmece
Contact Information
Primary
Hatice Zehra FERHATLAR
haticezehraferhatlar@gmail.com
+905367387869
Time Frame
Start Date: 2026-06-01
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 90
Treatments
Mild Carpal Tunnel Syndrome
Moderate Carpal Tunnel Syndrome
Severe Carpal Tunnel Syndrome
Sponsors
Leads: Kanuni Sultan Suleyman Training and Research Hospital

This content was sourced from clinicaltrials.gov