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Effect of TMS on Neuropathic Pain for Patients With Sci

A

Ankara Etlik City Hospital

Status

Enrolling

Conditions

Neuropathic Pain
Spinal Cord Injury

Treatments

Device: active TMS
Device: sham TMS

Study type

Interventional

Funder types

Other

Identifiers

NCT07293780
AEŞH-EK-2025-102

Details and patient eligibility

About

The aim of this study is to evaluate the efficacy of rTMS targeting the anterior cingulate cortex, another stimulation site that may be effective in the treatment of neuropathic pain, and to compare it with motor cortex stimulation.

Enrollment

39 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients for whom at least 12 months have passed since the date of the event
  2. Patients who meet the International Pain Working Group's criteria for central neuropathic pain below the level of the lesion and who have had pain for at least 6 months
  3. Patients aged 18-65
  4. Pain not attributable to other causes such as rheumatological diseases or diabetes
  5. Patients with VAS > 4 despite maximum dose of pharmacological agents (anticonvulsants, antidepressants, narcotics), exercise and physical therapy agents, taking into account renal function tests and other comorbidities

Exclusion criteria

  1. History of epilepsy
  2. Metallic implant in the scalp
  3. Cochlear implant
  4. Spinal cord stimulator
  5. Pacemaker
  6. Presence of psychiatric illness
  7. Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

39 participants in 3 patient groups

active rTMS primer motor cortex
Active Comparator group
Treatment:
Device: active TMS
rTMS anterior cingulate gyrus
Experimental group
Treatment:
Device: active TMS
sham rTMS primer motor cortex
Sham Comparator group
Treatment:
Device: sham TMS

Trial contacts and locations

2

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Central trial contact

Ayşe Naz Kalem Özgen, specialist

Data sourced from clinicaltrials.gov

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