"Ultrasound Measures and Clinical Outcomes in Healthy Individuals, Mild and Moderate Carpal Tunnel Syndrome Patients"

NCT07408596 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2026-02-13

No results posted yet for this study

Summary

"This study aims to investigate ultrasonographic parameters of the median nerve in healthy individuals and patients with mild and moderate carpal tunnel syndrome (CTS).

Specifically, investigator will assess the cross-sectional area (CSA) at the proximal carpal tunnel and the wrist/forearm ratio (WFR), and determine their diagnostic thresholds.

İnvestigators will also evaluate correlations between these ultrasound measures and clinical and electrophysiological findings, including pain, symptom severity, functional status, and quality of life (Visual Analog Scale, Boston Carpal Tunnel Questionnaire, SF-36).

Conditions

  • Carpal Tunnel Syndrome (CTS)
  • Median Nerve Entrapment
  • Electrophysiologic Study
  • Ultrasound
  • Ultrasound Diagnostics
  • Peripheral Nerve Disease
  • Peripheral Nerve Disorder
  • Entrapment Neuropathy, Carpal Tunnel
  • Entrapment Neuropathy

Interventions

DIAGNOSTIC_TEST

ultrasound

"We aim to determine whether carpal tunnel syndrome (CTS) can be accurately diagnosed using ultrasonographic parameters alone, and to what extent ultrasound-based parameters are consistent with electrodiagnostic (EMG) findings. Additionally, we seek to evaluate how the ultrasound parameters correlate with clinical outcomes, including functional status, quality of life, and pain severity."

Sponsors & Collaborators

  • Istanbul University

    lead OTHER

Principal Investigators

  • Demirhan Dıracoglu, Prof Dr · Istanbul Unıversity Istanbul Medicine Faculty

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-07-25
Primary Completion
2025-12-30
Completion
2025-12-30
FDA Device
Yes

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07408596 on ClinicalTrials.gov