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Clinical Trials in Turkey / NCT07167667
Recruiting Not applicable

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

NCT07167667 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-10-25
Last updated
2025-09-11

Condition(s) studied

Carpal Tunnel Syndrome (CTS)

Investigational drug(s) / intervention(s)

Paraffin BathExtracorporeal Shock Wave Therapy

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

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.

Study summary

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.

Eligibility

Sex
ALL
Min age
30 Years
Max age
60 Years
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Baltalimani Metin Sabanci Bone Diseases Training and Research Hospita Istanbul Turkey (Türkiye) Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07167667 on ClinicalTrials.gov ↗ ← All trials in Turkey