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RecruitingNCT07378046

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

The Analgesic Efficacy and Safety of Oral Medications (Baclofen) 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. Recent attention has focused on the potential role of muscle relaxant, which can relieve skeletal muscle spasms and associated pain in acute musculoskeletal conditions. Therefore, investigators hypothesize that baclofen may effectively reduce the severity of HZ pain without significantly increasing adverse events.

Conditions

Interventions

TypeNameDescription
DRUGBaclofen combined conventional therapyIn the baclofen combined conventional therapy group, baclofen will be initiated at 15 mg daily. Then, based on the patient's response, the single dose can be gradually increased by 5mg each time, with a three-day interval. The maximum recommended dose is 30\~75mg daily. In addition, the group will contain conventional treatment for HZ, except baclofen, including NSAIDs, opioids, antiviral drugs and so on.
DRUGConventional therapyIn the conventional therapy group, treatments will include NSAIDs, opioids, antiviral drugs and so on.

Timeline

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

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07378046. Inclusion in this directory is not an endorsement.