Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
ID06420778

Randomized Controlled Study of Superficial Needling Combined With Electroacupuncture for Treating Postherpetic Neuralgia in the Head and Face

Led by Zhejiang Chinese Medical University · Updated on 2025-04-06

124

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the treatment of postherpetic neuralgia (PHN) in the head and face area, focusing on whether superficial needling combined with electroacupuncture offers advantages in relieving pain, improving mood, sleep quality, and overall quality of life. The study also explores the use of infrared thermography to objectively assess treatment effects and aims to establish clinical standards for this acupuncture approach. Patients with head and face PHN who meet specific criteria are enrolled in this randomized controlled trial. Participants are assigned to one of two groups: the experimental group receives cluster needle shallow stabbing combined with electroacupuncture treatments lasting 60 minutes each, administered every other day, three times a week, for a total of 12 treatments over 4 weeks. The control group takes oral pregabalin capsules at a dose of 150 mg twice daily for 4 weeks. The study monitors both groups before treatment, immediately after the first treatment, and at multiple follow-up points extending to 2 months after treatment ends. During the study, participants undergo evaluations of pain severity using the Visual Analogue Scale (VAS) at baseline, 2 weeks, 1 month, and during follow-ups at 1 and 2 months post-treatment. Secondary assessments include depression scales, sleep quality indexes, and quality of life surveys administered at the same intervals. Infrared thermography is used to correlate facial temperature changes with clinical symptoms. Safety and treatment effects are closely monitored throughout the study period, with total participation lasting several months including follow-up.

CONDITIONS

Brief Title

The Treatment of Postherpetic Neuralgia in the Head and Face With Superficial Needling Combined With Electroacupuncture

Who Can Participate

Age: 50Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meet diagnostic criteria from the 2016 Chinese Expert Consensus on Postherpetic Neuralgia
  • Aged between 50 and 80 years
  • History of herpes zoster on head and face with healed lesions
  • Neuralgia symptoms lasting at least 1 month after lesions healed
  • Baseline Facial Pain Profile score of 4 or higher
  • Abnormal skin sensation and pain sensitivity around lesions
  • Conscious with clear pain and discrimination ability
  • Willing to sign informed consent voluntarily
Not Eligible

You will not qualify if you...

  • Do not meet diagnostic criteria for postherpetic neuralgia
  • Herpes zoster in perineum or special types like visceral, meningeal, or generalized herpes zoster
  • Taking oral pregabalin less than 0.2 g or more than 0.6 g daily before inclusion
  • Serious allergic reaction to pregabalin or acupuncture contraindications
  • Severe heart, liver, kidney damage, epilepsy, head injury, cognitive dysfunction, aphasia, psychiatric disorders, or inability to cooperate
  • Poorly controlled hypertension or diabetes
  • Pregnant or breastfeeding
  • Currently participating or enrolled in another clinical trial within last 3 months

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 4 weeks

Participants receive either superficial needling combined with electroacupuncture or oral pregabalin capsules for postherpetic neuralgia in the head and face.

Up to 12 treatments for needling and electroacupuncture (3 times per week); or twice daily oral medication for 4 weeks

Follow-up

Duration - 2 months

Participants are monitored to evaluate the lasting effects of treatment on pain, mood, sleep quality, and quality of life.

Visits at 1 month and 2 months after treatment ends

Trial Site Locations

Total: 1 location

1

Xiaoyu Li

Hangzhou, Zhejiang, China, 310053

Actively Recruiting

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Research Team

X

Xiaoyu Li

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

The efficacy of electroacupuncture for postherpetic neuralgia arising from herpes zoster affecting the cephalo-facial area: study protocol for a double center randomized controlled trial.

Pengfei Qiu, Haiju Sun, Yunfan Xia...

https://pubmed.ncbi.nlm.nih.gov/40950954