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Clinical Trials in Turkey / NCT06538779
Recruiting Observational

Sonographic Examination of Median Nerve Variations

NCT06538779 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-09-01
Last updated
2025-05-30

Condition(s) studied

Carpal Tunnel Syndrome

Investigational drug(s) / intervention(s)

elastography,usg

elastography,usg: Patients' general pain will be assessed with Visual Analog Scale (Global Pain), symptom severity and functional status will be assessed with Boston Carpal Tunnel Questionnaire, hand grip strength will be measured with dynamometer. Patient hand diagram will be marked according to patient's sensory symptoms. Median nerve cross-sectional area measurement at pisiform level with ultrasound, distal motor latency and sensory nerve conduction velocity with emg will be performed and recorded. Median nerve stiffness will be assessed with real-time elastography.

Study summary

The aim of the study is to evaluate the prevalence of bifid median nerve in patients diagnosed with carpal tunnel syndrome (CTS) and whether it has a higher prevalence in CTS patients than in asymptomatic individuals, and to evaluate the characteristics of the bifid median nerve found and whether median nerve variations are predisposing factors in the development of CTS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Having typical Carpal Tunnel Sydnrome symptoms lasting longer than 3 months * Carpal tunnel syndrome diagnosed with EMG * Being a male/female \>18 years of age Exclusion Criteria: * History of polyneuropathy, brachial plexopathy, thoracic outlet syndrome, or surgery in the wrist area * Presence of inflammatory arthritis, hypothyroidism, pregnancy, rheumatological disorders, diabetes mellitus * Presence of peripheral vascular disease

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Etlik City Hospital Ankara Ankara Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06538779 on ClinicalTrials.gov ↗ ← All trials in Turkey