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Trials / Recruiting

RecruitingNCT07370402

The Analgesic Efficacy and Safety of Flurbiprofen Patch in Patients With Herpes Zoster

The Analgesic Efficacy and Safety of Topical Patches (Flurbiprofen Patch) in Patients With Herpes Zoster

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
750 (estimated)
Sponsor
Beijing Tiantan Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Herpes zoster (HZ) is characterized by a painful dermatomal rash and significantly affects quality of life, with acute pain increasing the risk of postherpetic neuralgia. Although early antiviral therapy limits viral replication, its analgesic effect is insufficient, and many patients experience inadequate relief despite stepwise use of non-opioids and opioids. Topical NSAIDs offer a promising alternative by delivering localized analgesia with reduced systemic exposure. Therefore, investigators hypothesize that flurbiprofen patch may effectively reduce the severity of HZ pain without significantly increasing adverse events.

Conditions

Interventions

TypeNameDescription
DRUGFlurbiprofen patch combined with conventional therapy groupIn the flurbiprofen patch combined with conventional therapy group, apply the patch to the painful point near the herpes lesion. Use one patch per day, twice a day. In addition, the group will contain conventional treatment for HZ, except flurbiprofen patch, including opioids, antiviral drugs and so on.
DRUGConventional therapy groupIn the conventional therapy group, treatments will include opioids, antiviral drugs and so on.

Timeline

Start date
2025-12-15
Primary completion
2027-09-30
Completion
2027-12-31
First posted
2026-01-27
Last updated
2026-01-27

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07370402. Inclusion in this directory is not an endorsement.