Actively Recruiting

Phase Not Applicable
Age: 20Years - 90Years
All Genders
Healthy Volunteers
NCT06237075

Combining fMRI and tDCS in Neuropathic Pain

Led by National Taiwan University Hospital · Updated on 2024-02-01

150

Participants Needed

1

Research Sites

365 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The proposed project aims to explore possible neuromodulatory effects of transcranial direct current stimulation (tDCS) on neuropathic pain caused by peripheral neuropathy. tDCS will be performed through an MRI-compatible stimulation setting during functional magnetic resonance imaging (fMRI) scanning. The stimulation target of tDCS will be the primary motor cortex (M1) and the dorsolateral prefrontal cortex (DLPFC). We expect that results from the current project will advance the understanding of neuromodulatory mechanisms of tDCS and facilitate the development of treatment strategies for patients with neuropathic pain.

CONDITIONS

Official Title

Combining fMRI and tDCS in Neuropathic Pain

Who Can Participate

Age: 20Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 20 or older and 90 or younger
  • Ability to give informed consent
  • Neuropathic pain and/or nonpainful sensory symptoms caused by peripheral neuropathy confirmed by clinical symptoms, nerve conduction study, autonomic function test, quantitative sensory test, or skin biopsy
  • Stroke involving somatosensory pathway confirmed by neuroimaging
  • Agree not to consume caffeine, alcohol, tea, or drugs affecting the nervous system for 48 hours before each study session
Not Eligible

You will not qualify if you...

  • Severe systemic diseases such as severe ischemic heart disease or congestive heart failure (left ventricular ejection fraction < 30%), severe lung diseases with dyspnea, severe generalized edema, or systemic infection
  • Major neurological disorders including brain tumor, head trauma, or nervous system infection or inflammation
  • Major depression or other major mental disorders
  • Presence of cardiac pacemaker, brain stimulator, aneurysm clips, or metal implants in the head unless certified MRI-compatible
  • Pregnancy
  • Claustrophobia or other contraindications to MRI
  • Inability to give informed consent

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

National Taiwan University Hospital

Taipei, Taiwan, 112

Actively Recruiting

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Research Team

S

Sung-Tsang Hsieh, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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