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Clinical Trials in China / NCT07352553
Starting soon Not applicable

Brain Stimulation for Postherpetic Neuralgia: A Randomized Sham-Controlled Trial

NCT07352553 · tracked via the Priya Life Science China tracker
Sponsor
Huazhong University of Science and Technology
Phase
Not applicable
Started
2026-01-20
Last updated
2026-01-20

Condition(s) studied

Postherpetic Neuralgia

Investigational drug(s) / intervention(s)

Non-invasive transcranial stimulationSham Non-invasive transcranial stimulation

Non-invasive transcranial stimulation: Non-invasive transcranial stimulation is delivered once daily for 30 minutes for 10 consecutive days. Stimulation is administered using a multi-channel battery-powered device with five circular Ag/AgCl electrodes; current output is monitored in real time for safety.

Sham Non-invasive transcranial stimulation: Sham procedure with identical electrode placement and session duration (30 minutes once daily for 10 consecutive days). After an initial brief stimulation to mimic sensation, the current output is turned off.

Study summary

Pharmacotherapy is the cornerstone of Postherpetic Neuralgia (PHN) management. First-line treatments for PHN include antiviral agents (e.g., acyclovir, valacyclovir, famciclovir, and brivudine), centrally acting antiepileptic drugs (pregabalin and gabapentin), antidepressants (duloxetine and venlafaxine), and peripherally acting sodium-channel blockers (lidocaine patches).

In recent years, substantial progress has been made in the prevention and treatment of PHN, including early and active antiviral therapy (acyclovir, valacyclovir, famciclovir, brivudine, etc.), analgesic therapy (calcium-channel modulators such as pregabalin and gabapentin; tricyclic antidepressants such as amitriptyline; and opioid analgesics), interventional procedures (e.g., radiofrequency modulation and spinal cord stimulation), and vaccination. Nevertheless, clinical outcomes remain unsatisfactory, with the incidence of refractory PHN still exceeding 50%. Adverse effects associated with certain first- and second-line medications (such as antidepressants and anticonvulsants), as well as the potential risk of opioid dependence, markedly reduce treatment adherence. This situation has compelled clinicians to continually seek new and effective therapeutic approaches for PHN.

Non-invasive transcranial stimulation, as an emerging noninvasive neuromodulation technique, enables targeted modulation of deep brain structures. Animal studies have demonstrated that it can noninvasively regulate neuronal firing in deep regions and induce long-term plasticity, while offering relatively high spatial selectivity and tissue penetration. These features suggest broad clinical potential in chronic pain and affective disorders.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years. * Diagnosis of postherpetic neuralgia (PHN) with disease duration ≥ 3 months. * NRS pain score ≥ 4. * Willing to receive the intervention and able to provide written informed consent. Exclusion Criteria: * Contraindications to electrical stimulation (e.g., intracranial metal implants, cardiac pacemaker). * History of epilepsy, severe psychiatric disorder, or cognitive impairment. * Pregnant or breastfeeding women. * Unable to comply with the intervention procedures and follow-up assessments.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tongji hospital Wuhan Hubei

More Huazhong University of Science and Technology trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07352553 on ClinicalTrials.gov ↗ ← All trials in China