Clinical Trial

The Analgesic Efficacy and Safety of Tulodesvenlafaxine in Patients With Herpes Zoster

Recruiting
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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. Recent attention has focused on the potential role of antidepressants, which have central antinociceptive property and may offer analgesic benefits by modulating central nervous system pain pathways through increased serotonin and norepinephrine availability. Therefore, investigators hypothesize that tulodesvenlafaxine may effectively reduce the severity of HZ pain without significantly increasing adverse events.
Trial Details
NCT Number NCT07370389
Lead Sponsor Beijing Tiantan Hospital
Conditions Herpes Zoster, Pain
Enrollment 750 participants
Start Date 2025-12-15
Primary Completion 2027-09-30 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-01-27