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Study on the correlation between fire-needle pain and analgesic effect in treating acute herpes zoster

Study on the correlation between fire-needle pain and analgesic effect in treating acute herpes zoster

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046426
Enrollment
Unknown
Registered
2021-05-15
Start date
2021-05-15
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

Acute herps zoster

Interventions

Sponsors

South District of Guang'anmen Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for herpes zoster; 2. Aged range from 18 to 75 years; 3. No antiviral drugs or analgesics have been taken or used externally within 1 week; 4. Neuropathic pain vas value >= 50%; 5. Sign the informed consent form and volunteer to participate in this research.

Exclusion criteria

Exclusion criteria: 1. Special types, such as meningeal herpes zoster, visceral herpes zoster, eye and ear herpes zoster, generalized herpes zoster, non-rash type herpes zoster, etc.; 2. Patients who are highly allergic to amide local anesthetics or to any other ingredients in compound lidocaine cream; 3. Long-term use of corticosteroids or immunosuppressive agents; 4. Patients with congenital or idiopathic methemoglobinemia; 5. Women who are breastfeeding, pregnant or preparing to become pregnant; 6. Patients with severe primary diseases or systemic failure such as cardiovascular, cerebrovascular, liver, kidney, hematopoietic system, patients with atopic dermatitis, psychiatric patients, hemophilia patients, and patients with bleeding tendency; 7. Patients who are in a critical condition and are difficult to make an accurate assessment of the effectiveness and safety of the treatment; 8. Patients with scar constitution.

Design outcomes

Primary

MeasureTime frame
The change of the VAS score from baseline in the most painful degree of acute neuralgia in local herpes zoster;

Secondary

MeasureTime frame
The time required for constant pain intensity of VAS below 30%;Percentage of patients with the most painful VAS score of herpes zoster acute neuralgia decreased to less than 30%;

Countries

China

Contacts

Public ContactGuo Yufeng

Guang'anmen Hospital, China Academy of Traditional Chinese Medicine

gamgyf@139.com+86 18511664134

Outcome results

None listed

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