Duloxetine for PHN

NCT04313335 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 750

Last updated 2024-01-09

No results posted yet for this study

Summary

In this study, the investigators aim to investigate the preventive efficacy of prophylactic oral duloxetine during acute herpes zoster on postherpetic neuralgia and its safety.

Conditions

  • Postherpetic Neuralgia

Interventions

DRUG

Duloxetine

Oral Duloxetine (up to 60 mg per day) will be given, titrated, tapered in accordance with the pain intensity during the acute herpes zoster period.

Sponsors & Collaborators

  • China-Japan Friendship Hospital

    collaborator OTHER
  • Tianjin Medical University Second Hospital

    collaborator OTHER
  • Taiyuan Central Hospital of Shanxi Medical University

    collaborator OTHER
  • Linfen Fourth People's Hospital

    collaborator UNKNOWN
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • Qingdao Municipal Hospital (Group)

    collaborator UNKNOWN
  • The Second People's Hospital of Huai'an

    collaborator OTHER
  • First Hospital of China Medical University

    collaborator OTHER
  • Second Affiliated Hospital of Zhengzhou University

    collaborator OTHER
  • Fujian Provincial Hospital

    collaborator OTHER
  • Cangzhou Central Hospital

    collaborator OTHER
  • The People's Hospital of Fujian Province

    collaborator UNKNOWN
  • Beijing Tsinghua Chang Gung Hospital

    collaborator OTHER
  • Peking University International Hospital

    collaborator OTHER
  • Tianjin First Central Hospital

    collaborator OTHER
  • Tianjin Huanhu Hospital

    collaborator OTHER
  • Baoding First Central Hospital

    collaborator OTHER
  • Beijing Tiantan Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-01
Primary Completion
2023-05-16
Completion
2023-05-16

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04313335 on ClinicalTrials.gov