Skip to content

ZAP(subacute stage) lesion site IRT changes and acupuncture based electroacupuncture intervention effect of multi-center RCT study

Clinical study on optimal evaluation of acupuncture treatment for herpes zoster neuralgia based on changes in biological characteristics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000883
Enrollment
Unknown
Registered
2025-05-01
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

zoster-associated pain

Interventions

control group:sham electro acupuncture plus pregabalin
treatment group:electroacupuncture plus pregabalin

Sponsors

Hangzhou Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria for subacute ZAP ; (2) The baseline score of local pain conditions is greater than or equal to 4 points but no more than 7 points; (3) neuralgia caused by shingles of the trunk; (4) Age 18-85 years old (including end value) gender is not limited; (5) clear consciousness pain perception and discrimination ability no basic communication barriers; (6) Voluntarily participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Those who do not meet the above inclusion criteria; (2) herpes zoster occurring on the head and face limbs or combined generalized zoster or other special types of zoster such as meningozoster visceral zoster; (3) pregnant and lactating patients; (4) Patients allergic to pregabalin or acupuncture stimulation; (5) Patients with severe organ damage or cognitive dysfunction mental disorder aphasia or other major diseases unable to cooperate with treatment; (6) combined with other serious skin diseases; (7) Patients with cardiac pacemakers; (8) Within the last 3 months or currently participating in other clinical investigators.

Design outcomes

Secondary

MeasureTime frame
Infrared thermograph;Self-Rating Anxiety Scale;Medical Outcomes Study-Sleep Scores;Self-Rating Depression Scale;Brief Pain Inventory;Short Form 36-item Health Survey;

Primary

MeasureTime frame
visual analogue scale;

Countries

China

Contacts

Public ContactZhang Zuyong

Hangzhou Third People's Hospital

20168028@zcmu.edu.cn+86 135 1682 5005

Outcome results

None listed

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