Investigation of the Relationship Between Pain Sensitization and Diagnostic Parameters in Carpal Tunnel Syndrome
NCT ID: NCT06043141
Last Updated: 2025-09-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
60 participants
OBSERVATIONAL
2023-10-01
2025-05-30
Brief Summary
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The main questions it aims to answer are:
* Can threshold values be determined ultrasonographically and electrodiagnostically in patients who develop pain sensitization?
* Are pressure pain threshold values and central sensitization inventory scores correlated with ultrasonographic and nerve conduction studies of the median nerve?
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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Patients with carpal tunnel syndrome
Patients with carpal tunnel syndrome
Nerve ultrasound
Ultrasonographic evaluation of the median nerve at the carpal tunnel and adjacent levels
Nerve conduction studies
Upper extremity nerve conduction studies including median-ulnar sensory and motor responses
Pressure pain threshold
Pain pressure threshold (PPT) is used to measure deep muscular tissue pain sensitivity.
Control group
Healthy control
Nerve ultrasound
Ultrasonographic evaluation of the median nerve at the carpal tunnel and adjacent levels
Pressure pain threshold
Pain pressure threshold (PPT) is used to measure deep muscular tissue pain sensitivity.
Interventions
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Nerve ultrasound
Ultrasonographic evaluation of the median nerve at the carpal tunnel and adjacent levels
Nerve conduction studies
Upper extremity nerve conduction studies including median-ulnar sensory and motor responses
Pressure pain threshold
Pain pressure threshold (PPT) is used to measure deep muscular tissue pain sensitivity.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Agreeing to participate in the study
Exclusion Criteria
* Having a disease with neuropathic pain such as polyneuropathy, radiculopathy,multiple sclerosis
* Not agreeing to participate in the study
* History of surgery due to CTS
18 Years
65 Years
ALL
No
Sponsors
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Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
OTHER
Responsible Party
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Feyza Nur Yucel
Specialist
Principal Investigators
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Emre Ata, Asst.Prof
Role: STUDY_CHAIR
Saglik Bilimleri Universitesi
Locations
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Sultan Abdülhamid Han Training and Research Hospital
Istanbul, Uskudar, Turkey (Türkiye)
Countries
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Other Identifiers
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23-517
Identifier Type: -
Identifier Source: org_study_id
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