Skip to content
Not yet recruitingPhase 4

Ketamine for Postherpetic Neuralgia With Depression

NCT06968624 · Huazhong University of Science and Technology

Closed to entry
Status
Not accepting participants
Phase 4
Phase
50
Target enrolment
Study sites

What it is testing

Summary

This clinical trial examines the antidepressant efficacy and safety of a single low-dose intravenous esketamine combined with oral duloxetine in patients with postherpetic neuralgia and depression (duration more than 1 month). In this prospective, randomized, double-blind, placebo-controlled parallel study, eligible patients were randomized into two groups: one received esketamine plus duloxetine, and the other got placebo plus duloxetine. Both groups underwent standard pain management and neuro modulation therapy. The primary outcome was the Hospital Anxiety and Depression Scale - Depression( HADS-D)score at 2 weeks post - infusion, with various secondary outcomes assessed over multiple time points. Data were collected through in-person interviews and telephone follow-ups.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Hospital Anxiety and Depression Scale - Depression score

    Measured over 2 weeks after intravenous ketamine infusion therapy

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years to 65 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Diagnosed with herpetic neuralgia, with a disease course exceeding 1 month, and an HADS-D score ≥8 (15) upon admission. * Diagnosed with depression based on the DSM-V and ICD-11 criteria. * Aged between 18 and 65 years old. * BMI \<30 kg/m². Exclusion Criteria: * Unable to cooperate with questionnaires. * Allergic to ketamine. * History of other mental disorders such as anxiety. * Severe hypertension and serious dysfunctions of heart, lung, liver, or kidney.

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT06968624 on ClinicalTrials.gov →

Last updated in the registry 2025-06-03. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits