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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-60
SponsorEmre Şenocak

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.

Eligibility criteria

Qualifiers

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)

Disqualifiers

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,

Trial design

Treatments tested in this trial

  • Paraffin Bath
  • Extracorporeal Shock Wave Therapy

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Emre Şenocak

Lead sponsor

Karadeniz Technical University

Sponsor institution