RECRUITINGINTERVENTIONAL

Median Nerve Thickness of the Carpal Tunnel Syndrome After Two Different Physiotherapy Modalities

Investigation of the Effects of Two Different Physiotherapy Modalities on Median Nerve Thickness, Electrophysiological Activity, Pain Intensity and Quality of Life in Patients With Carpal Tunnel Syndrome - An Observational Study

About This Trial

The study plans to include a total of 60 patients diagnosed with carpal tunnel syndrome. Patients will be divided into two groups according to the treatment they receive. One group will receive only paraffin treatment, while the other group will receive only ESWT treatment. ESWT will be applied for a total of 5 sessions. Paraffin will be applied for a total of 10 sessions. As assessment tools; * Measurement of median nerve thickness with ultrasound * Electromyography * Visual Analog Scale * Short Form-36 Evaluations will be made twice by a specialist physician before and after the treatments.

Who May Be Eligible (Plain English)

Who May Qualify: - Individuals between the ages of 30-60 who have been diagnosed with CTS by a specialist physician according to international criteria (Those between Stages 1-3), - Those who have complaints of numbness, tingling, and pain in the first three fingers and half of the fourth finger, - Phalen Test and Tinel sign or Durkan Test being positive - Patients who will receive 5 sessions of ESWT application prescribed by a Physical Medicine and Rehabilitation Specialist Physician (for the ESWT group) - Patients who have been recommended 10 sessions of Paraffin application by a Physical Medicine and Rehabilitation Specialist Physician (for the Paraffin group) Who Should NOT Join This Trial: - Presence of atrophy in the thenar muscles, - Insufficient sensory and motor response in the median nerve, - History of hand and/or wrist injury or surgery, - Those with cervical stenosis, cervical spondylosis, or cervical radiculopathy, - Corticosteroids in the carpal tunnel area within the last six months those who have had an injection, - Pregnancy or diabetes, renal failure, rheumatoid arthritis or hypothyroidism Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language

Inclusion Criteria: * Individuals between the ages of 30-60 who have been diagnosed with CTS by a specialist physician according to international criteria (Those between Stages 1-3), * Those who have complaints of numbness, tingling, and pain in the first three fingers and half of the fourth finger, * Phalen Test and Tinel sign or Durkan Test being positive * Patients who will receive 5 sessions of ESWT application prescribed by a Physical Medicine and Rehabilitation Specialist Physician (for the ESWT group) * Patients who have been recommended 10 sessions of Paraffin application by a Physical Medicine and Rehabilitation Specialist Physician (for the Paraffin group) Exclusion Criteria: * Presence of atrophy in the thenar muscles, * Insufficient sensory and motor response in the median nerve, * History of hand and/or wrist injury or surgery, * Those with cervical stenosis, cervical spondylosis, or cervical radiculopathy, * Corticosteroids in the carpal tunnel area within the last six months those who have had an injection, * Pregnancy or diabetes, renal failure, rheumatoid arthritis or hypothyroidism

Treatments Being Tested

OTHER

Paraffin Bath

Patients' hands will be dipped into the paraffin bath 8-10 times.

OTHER

Extracorporeal Shock Wave Therapy

The patients will be treated with a sound wave pulse frequency of 15 Hz, an intensity of 1.5 bar, and a total number of pulses of 2000 for one session.

Locations (1)

Baltalimani Metin Sabanci Bone Diseases Training and Research Hospita

Istanbul, Turkey (Türkiye)