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An observational cohort study of the efficacy and safety of crisugabalin besilate capsules for the treatment of patients with acute herpes zoster in the real world

An observational cohort study of the efficacy and safety of crisugabalin besilate capsules for the treatment of patients with acute herpes zoster in the real world

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101244
Enrollment
Unknown
Registered
2025-04-22
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Acute herpes zoster

Interventions

Crisugabalin Besilate Capsules Group:NA

Sponsors

Hangzhou Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Able to understand and voluntarily sign a written informed consent form (ICF); 2.Age >= 50 years old; 3.Diagnosed with acute herpes zoster; 4.Presents with vesicles within 7 days; 5.Average pain visual analog scale (VAS) score >= 40 mm in the past 24 h assessed at screening.

Exclusion criteria

Exclusion criteria: 1.Participation in any other clinical study within 30 days prior to screening; 2.HZ vaccinated; 3.Received minimally invasive interventions with analgesic effects such as nerve block,nerve destruction, spinal cord stimulation, electrical stimulation, etc.; 4.Immunocompromised: mainly HIV/AIDS, malignant tumors, organ transplantation,stem cell transplantation patients,and long-term immunosuppressant treatment, etc.; 5.Ocular herpes zoster; 6.Other conditions that, in the judgement of the investigator, make participation in this study inappropriate.

Design outcomes

Primary

MeasureTime frame
Incidence of PHN;NRS scores;

Countries

China

Contacts

Public ContactJianming Yu

Hangzhou Third People's Hospital

hhkjyjm@163.com+86 13750840613

Outcome results

None listed

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