Investigation of the Relationship Between Ultrasonographic Parameters and Tactile Sensation in Carpal Tunnel Syndrome

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorSultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

About this trial

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?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Electrodiagnostic diagnosis of carpal tunnel syndrome with pain, numbness, burning, and tingling consistent with the median nerve dermatomal area lasting at least 6 weeks.

Literate

Agree to participate in the study

Disqualifiers

Concomitant diabetes, systemic inflammatory disease, active infection, and history of malignancy

Being <18 and >65 years old

Being illiterate

Refusing to participate in the study

Trial population

Patients with diagnosed CTS

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Nerve conduction studies

    Diagnostic test

    Upper extremity nerve conduction studies including median-ulnar sensory and motor responses

  • Median nerve ultrasonography

    Diagnostic test

    Median nerve sonographic cross-sectional area and echogenicity measurements

  • Sensory testing

    Diagnostic test

    tactile sensory tests

Treatment groups

84 Participants
are divided into 1 treatment group
Group A: Patient group3 interventions

Trial outcomes

Primary outcomes

1

median nerve ultrasound

Median nerve maximum cross-sectional area measurement at the level of the carpal tunnel (mm²)

Time frame
3 Months
2

Pointed - blunt discrimination test

The patient is asked to distinguish between a pointed and a blunt tip by touching the median nerve dermatome.

Time frame
3 Months
3

Moved two point discrimination

The patient's finger is touched, starting from the distal tip and moving proximally, and the patient is asked to distinguish between one and two dots. The distance between the last pair of dots the patient can distinguish is noted in mm.

Time frame
3 months
4

Fixed Two Point Discrimination Test

The patient's finger is touched starting from the distal tip and working proximally, and the patient is asked to distinguish between one and two dots. The distance between the last pair of dots the patient can distinguish is noted in millimeters.

Time frame
3 months

Secondary outcomes

1

Boston Carpal Tunnel Syndrome Questionnaire

The scale consists of an 11-question Likert-style symptom severity scale and an 8-question functional status scale. The total score is divided by the number of questions to calculate the score. Higher scores are associated with increased symptom severity and poorer functional status.

Time frame
3 Months
2

S-LANSS

A score of 12 or more out of 24 on a 7-question scale is considered in favor of neuropathic pain.

Time frame
3 Months
3

SF-12 (Short Form-12)

The SF-12 is a practical test consisting of seven questions that examine the life limits of the patient. The questionnaire includes questions aimed at understanding the physical and psychiatric effects. The results of the survey are calculated using two score calculation tools: physical (PCS-12) and mental (MCS-12). The highest score for the PCS-12 is 56.6, while the highest score for the MCS-12 is 60.7. Higher scores are comparable to a state of resilience and recovery, which can be compared to quality of life.

Time frame
3 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.