Actively Recruiting
Investigation of the Relationship Between Ultrasonographic Parameters and Tactile Sensation in Carpal Tunnel Syndrome
Led by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey · Updated on 2025-09-12
84
Participants Needed
1
Research Sites
38 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study was to investigate the relationship between different ultrasonographic indices used in patients with carpal tunnel syndrome and the level of tactile sensation. The primary questions the study aimed to answer are: • To what extent are the ultrasonographic parameters used in the diagnosis of carpal tunnel syndrome related to the level of sensory complaints in the patient?
CONDITIONS
Official Title
Investigation of the Relationship Between Ultrasonographic Parameters and Tactile Sensation in Carpal Tunnel Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of carpal tunnel syndrome confirmed by electrodiagnostic tests with symptoms such as pain, numbness, burning, or tingling in the median nerve area lasting at least 6 weeks
- Ability to read and write
- Willingness to participate in the study
You will not qualify if you...
- Having diabetes, systemic inflammatory disease, active infection, or history of cancer
- Being younger than 18 or older than 65 years
- Illiteracy
- Declining to participate in the study
- Having neuropathic pain conditions like polyneuropathy, radiculopathy, or multiple sclerosis
- Having other upper extremity nerve entrapment disorders such as cubital tunnel syndrome
- Previous surgery for carpal tunnel syndrome
- Rheumatoid arthritis or advanced hand osteoarthritis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sultan Abdülhamit Han Trainin and Educational Hospital
Üsküdar, İ̇stanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
M
Müyesser Cavlak, PhD
CONTACT
F
Feyza Nur Yücel, Specialist
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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