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A Study on the Application of Xia Tian Wu Injection (formerly known as Pudilan) in Neuroblockade Analgesia

An Efficacy Evaluation Study of Applying Xia Tian Wu Injection (formerly known as Pudilan) for Neuroblockade Analgesia in Patients with Herpes Zoster

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080319
Enrollment
Unknown
Registered
2024-01-26
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

Herpes Zoster

Interventions

experimental group:In accordance with the neural distribution of herpes zoster lesions, administer XiaTianWu injection 4 ml around the affected nerve every other day, for a total of 5 treatments
Control Group:The control group received intravenous infusion of acyclovir at a daily dose of 0.5 grams for a duration of 7 consecutive days.

Sponsors

Strategic Support Force Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age greater than or equal to 18 years and less than or equal to 80 years. 2.Patients with herpes zoster, diagnosed based on the typical clinical manifestations of herpes zoster, following the criteria outlined in the "Chinese Expert Consensus on Diagnosis and Treatment of Herpes Zoster 2022." 3.Visual Analogue Scale (VAS) score greater than 3. 4.Voluntary participation in this trial.

Exclusion criteria

Exclusion criteria: 1.Pregnancy. 2.Fasting blood glucose level greater than 8.8 mmol/L. 3.Poorly controlled hypertension, with systolic blood pressure greater than 180 mmHg and/or diastolic blood pressure greater than 120 mmHg. 4.Age less than 18 years or greater than 75 years. 5.Patients with visceral organic lesions requiring urgent intervention. 6.Patients with fractures, ligament tears, or other injuries requiring emergency surgery. 7.Patients with neurological tumors. 8.Patients taking oral anticoagulants. 9.Non-voluntary participation in this trial. 10.Numeric Rating Scale (NRS) pain score less than or equal to 3.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale,VAS;

Secondary

MeasureTime frame
herpes scabbing time;

Countries

China

Contacts

Public ContactGuoxin Han

Strategic Support Force Medical Center

hgx0536@163.com+86 157 0160 9710

Outcome results

None listed

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