Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT07114913

Symptom Distribution and Pain Sensitization in Carpal Tunnel Syndrome

Led by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey · Updated on 2025-08-11

80

Participants Needed

1

Research Sites

36 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to compare central sensitization parameters between carpal tunnel syndrome (CTS) patients with extra median symptom distribution and those with typical, median nerve-related symptoms. Extra median sensory spread, observed in some CTS patients beyond the anatomical boundaries of the median nerve, may reflect central sensitization mechanisms. Using the Central Sensitization Inventory and pressure pain threshold measurements, this study will assess whether extra median symptom patterns are associated with increased central sensitization.

CONDITIONS

Official Title

Symptom Distribution and Pain Sensitization in Carpal Tunnel Syndrome

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with carpal tunnel syndrome based on clinical and electrodiagnostic findings
  • Aged between 18 and 65 years
  • Able to read and write
  • Agreeing to participate in the study
Not Eligible

You will not qualify if you...

  • History of diabetes, systemic inflammatory disease, active infection, or malignancy
  • Younger than 18 or older than 65 years
  • Illiterate
  • Refusal to participate in the study
  • Having neuropathic pain conditions like polyneuropathy, radiculopathy, or multiple sclerosis
  • Injection or surgery for carpal tunnel syndrome within the last 6 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sultan Abdülhamid Han Training and Research Hospital

Istanbul, Usküdar, Turkey (Türkiye), 34100

Actively Recruiting

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Research Team

F

Feyza Nur Yücel, Specialist

CONTACT

E

Emre Ata, Assoc. Prof

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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