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A randomized controlled trial study of electroacupuncture for pain improvement in patients with postherpetic neuralgia

A randomized controlled trial study of electroacupuncture for pain improvement in patients with postherpetic neuralgia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068878
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

postherpetic neuralgia

Interventions

Experimental group:electroacupuncture

Sponsors

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age over 50 years. 2. Meet the diagnostic criteria for postherpetic neuralgia in the 2016 Chinese Expert Consensus on the Treatment of Postherpetic Neuralgia by the Consensus Writing Expert Group on the Treatment of Postherpetic Neuralgia. 3. Patients with PHN agree to receive acute analgesics. 4. The average maximum pain level VAS >= 3 points within 1 week of the screening period. 5. Patients themselves signed the informed consent form and voluntarily participated in this trial.

Exclusion criteria

Exclusion criteria: 1. PHN with previous neurolytic block or neurosurgical treatment. 2. severe pain or neurological disorders unrelated to PHN or the presence of skin changes other than PHN that can cause pain. 3. Patients with mood disorders requiring tricyclic antidepressants, and those with mental and intellectual impairment unable to cooperate with questionnaires. 4. Combined with serious primary diseases such as cardiovascular, cerebrovascular, hepatic, renal and hematopoietic system and other organic lesions such as tumors. 5. Pregnant and lactating women, and those who have a request for childbirth in the last six months. 6. Poorly controlled blood sugar, glycosylated hemoglobin >= 8.0% 7. Patients with immunodeficiency diseases such as pernicious anemia, untreated hypothyroidism or history of HIV infection and history of positive hepatitis B antigen or hepatitis C antibody, active tuberculosis, etc. 8. Patients who have received previous acupuncture treatment. 9.Patients belonging to the vulva and brachial plexus region and special types of herpes zoster, where special types include: ocular and ear herpes zoster, herpes zoster with stenosis, herpes zoster without rash, herpes zoster meningitis or encephalitis, herpes zoster invading visceral nerve fibers, disseminated herpes zoster and other (herpes zoster with maculopapular, hemorrhagic, gangrenous and other manifestations) resulting in PHN. 10. Concurrent participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
VAS responder rate(>=50%);

Secondary

MeasureTime frame
Intensity of acute zoster-associated pain;McGill Pain Questionnaire;BPI-SF;Time to relieving of pain;Average daily sleep interference score;PGIC;hospital anxiety and depression scale;36- item short form health survey;

Countries

China

Contacts

Public ContactBin Li

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University

libin@bjzhongyi.com+86 189 1078 1852

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026