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Recruiting NCT06237075

NCT06237075 Combining fMRI and tDCS in Neuropathic Pain

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Clinical Trial Summary
NCT ID NCT06237075
Status Recruiting
Phase
Sponsor National Taiwan University Hospital
Condition Neuropathic Pain
Study Type INTERVENTIONAL
Enrollment 150 participants
Start Date 2023-09-11
Primary Completion 2030-09-11

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 90 Years
Study Type INTERVENTIONAL
Interventions
transcranial direct current stimulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 150 participants in total. It began in 2023-09-11 with a primary completion date of 2030-09-11.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * 1\. Age 20 or older and 90 or younger. 2. Ability to give informed consent 3. Neuropathic pain and/or nonpainful sensory symptoms resulted from I or II I. Peripheral neuropathy confirmed by clinical symptoms nerve conduction study, autonomic function test, quantitative sensory test, or skin biopsy. II. Stroke involving somatosensory pathway confirmed by neuroimage 4. Agree not to take caffeine, alcohol, tea and drugs with significant nervous system effects for 48 hours before each study session. Exclusion Criteria: * 1\. Presence of sever systemic diseases, including severe ischemic heart disease or congestive heart failure (left ventricular ejection fraction \< 30%), severe lung diseases with dyspnea, severe generalized edema, and systemic infection 2. Presence of major neurological disorders, including brain tumor, head trauma and infection or inflammation of nervous system. 3\. Presence of major depression or any major mental disorders 4. Presence of a cardiac pacemaker, brain stimulator, aneurysm clips or metal implants in the head, unless these devices are certified to be MRI-compatible 5. Pregnancy 6. Claustrophobia or any other contraindications to MRI 7. Inability to give informed consent.

Contact & Investigator

Central Contact

Sung-Tsang Hsieh, MD, PhD

✉ shsieh@ntu.edu.tw

📞 (886)-2- 2-2312-3456

Frequently Asked Questions

Who can join the NCT06237075 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 90 Years, studying Neuropathic Pain. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06237075 currently recruiting?

Yes, NCT06237075 is actively recruiting participants. Contact the research team at shsieh@ntu.edu.tw for enrollment information.

Where is the NCT06237075 trial being conducted?

This trial is being conducted at Taipei, Taiwan.

Who is sponsoring the NCT06237075 clinical trial?

NCT06237075 is sponsored by National Taiwan University Hospital. The trial plans to enroll 150 participants.

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