Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06726954

Repetitive Transcranial Magnetic Stimulation Therapy in Spinal Cord Injury Related Neuropathic Pain

Led by Afyonkarahisar Health Sciences University · Updated on 2026-03-09

63

Participants Needed

1

Research Sites

93 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of our study is to investigate the effect of different protocols of high-frequency Repetitive Transcranial Magnetic Stimulation (rTMS) therapy added to the rehabilitation program on neuropathic pain,depression, quality of life and quality of sleep compared to each other and placebo group in participants with spinal cord injury.

CONDITIONS

Official Title

Repetitive Transcranial Magnetic Stimulation Therapy in Spinal Cord Injury Related Neuropathic Pain

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 75 years
  • Physician-diagnosed spinal cord injury for at least 3 months
  • Neuropathic pain present for at least 3 months
  • Pain not caused by other conditions
Not Eligible

You will not qualify if you...

  • Severe heart disease such as aortic stenosis, angina, hypertrophic cardiomyopathy, uncontrolled hypertension, arrhythmia, or having a pacemaker
  • Neurodegenerative disease
  • Epilepsy or history of antiepileptic drug use
  • Cognitive dysfunction
  • Lower extremity peripheral nerve injury
  • Increased intracranial pressure or uncontrolled migraine
  • Skin infection at the treatment area
  • Brain lesion or history of drug use affecting seizure threshold
  • Any contraindications to TMS including pacemaker or metallic implant
  • Previous seizure
  • Psychiatric disorders except depression and anxiety
  • Malignancy
  • Current pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Afyonkarahisar Health Sciences University

Afyonkarahisar, Turkey (Türkiye), 0300

Actively Recruiting

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Research Team

A

Ayse Kalender, MD

CONTACT

N

Nuran Eyvaz, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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