Acute Herpes Zoster

3

Review clinical trials related to Acute Herpes Zoster. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Midpoint Transverse Process to Pleura (MTP) Block vs Erector Spinae Plane (ESP) Block for Acute Herpes Zoster (HZ) Pain

The aim of this study is to compare the analgesic efficacy and safety of ultrasound-guided midpoint transverse process block versus ultrasound-guided erector spinae plane block in patients suffering from thoracic herpes zoster pain.

Participants needed: 90
Trial details
Age: 21-60Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jul 29, 2026Locations: 1
Eligibility criteria

Age 21-60 years. [+4]

Refusal to participate. [+9]

Status: Recruiting

Subcutaneous Calcitonin in Acute Herpes Zoster

This prospective randomized controlled study will be conducted to evaluate the effect of adding calcitonin to the standard treatment protocol in patients with acute herpes zoster infection.

Participants needed: 168
Trial details
Phase: Phase 3Age: 50+Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jul 6, 2026Locations: 1
Eligibility criteria

patients aged ≥ 50 years, with acute herpes zoster infection (rash duration < 7...

Coagulation abnormalities [+3]

Status: Recruiting

Efficacy of Electroacupuncture for Acute Herpes Zoster-Associated Pain and Biomarker Evaluation

Background: Herpes zoster (HZ) is an acute dermatological condition caused by the varicella-zoster virus. Its onset is characterized by severe pain, imposing significant physical and psychological burdens on patients. Acupuncture offers distinct advantages in treating acute herpes zoster and associated pain. However, the therapeutic efficacy of electroacupuncture for acute herpes zoster, its potential to reduce PHN incidence, and the role of biomarkers in predicting PHN incidence require further clinical validation. Methods: A total of 228 patients with acute herpes zoster will be recruited from 3 hospitals and randomly assigned to EA group or medication-alone group or sham acupuncture group in a 1:1:1 ratio, utilizing multicenter stratified block randomization. The trial will involve a 2 week treatment period, and a 3-month follow-up period. All variables will be evaluated at week 0, week 1, week 2, and on the 90th day after rash onset. All participants will continue antiviral medication treatment. Primary outcome is Numerical Rating Scale; secondary outcomes include herpes lesion crusting time, pain episodes within a 24-hour period, Hamilton Anxiety Scale, Hamilton Depression Scale, 36-Item Short Form Health Survey, changes of biomarkers (Erythrocyte sedimentation rate, C-reactive protein, Tumor Necrosis Factor-α, Interleukin-10, Substance P and neuropeptide Y) and PHN incidence rate. All adverse effects will be assessed during the trial. Conclusion: This study will elucidate the efficacy of electroacupuncture in treating acute herpes zoster, whether electroacupuncture can reduce the incidence of PHN, and the role of biomarkers in predicting the incidence of PHN.

Participants needed: 228
Trial details
Age: 20-80Biological sex: AllType: InterventionalSponsor: Dexiong HanUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Patients who meet the diagnostic criteria for acute HZ27 and skin symptom appear... [+1]

Special types of HZ that occur in head, eyes, viscera, etc. or those combined wi... [+8]