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Clinical Trials/NCT06449547
NCT06449547
Recruiting
Not Applicable

Risk Factors Analysis of Anxiety and Depression in Patients With Herpes Zoster Neuralgia and Characteristics of Serum Biomarkers and Functional Brain Magnetic Resonance Changes

Huazhong University of Science and Technology1 site in 1 country600 target enrollmentJune 21, 2024
ConditionsHerpes Zoster

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Herpes Zoster
Sponsor
Huazhong University of Science and Technology
Enrollment
600
Locations
1
Primary Endpoint
HADS score
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this observational study is to explore risk factors of anxiety and depression in patients with herpes zoster neuralgia, and the changes of certain serum biomarkers and functional brain magnetic resonance images of these patients.

Detailed Description

Patients with herpes zoster neuralgia will be recruited and take Hospital anxiety depression rating scale (Hospital anxiety and 'scale, HADS) evaluation. According to the HADS Scores, patients will be divided into depression group and no depression, or anxiety group and no anxiety group. The clinical data the of two groups will be collected and statistically analyzed to explore the risk factors of anxiety and depression, including the changes of serum biomarkers and functional brain magnetic resonance imaging in patients with herpes zoster neuralgia accompanying anxiety or depression.

Registry
clinicaltrials.gov
Start Date
June 21, 2024
End Date
December 2026
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wei Mei

Deputy director of anesthesiology

Huazhong University of Science and Technology

Eligibility Criteria

Inclusion Criteria

  • Age more than 18 years old
  • Diagnosed as herpes zoster neuralgia
  • Signing informed consent

Exclusion Criteria

  • Unable to complete the scale assessment
  • History of mental illness

Outcomes

Primary Outcomes

HADS score

Time Frame: during hospital stay, average of 1 week

Enrolled patients will be first evaluated by Hospital Anxiety and Depression Scare questionaire and according to the HADS score, patients will be divided to group with anxiety/depression and group without anxiety/depression.

Secondary Outcomes

  • Interleukin (IL)-1β plasma level(during hospital stay, average of 1 week)
  • C-reactive protein (CRP) plasma level(during hospital stay, average of 1 week)
  • Area under curve (AUC) of topological metrics of functional brain magnetic resonance imaging(during hospital stay, average of 1 week)
  • IL-2 receptor plasma level(during hospital stay, average of 1 week)
  • IL-10 plasma level(during hospital stay, average of 1 week)
  • Interferon(INF)-α plasma level(during hospital stay, average of 1 week)
  • IL-8 plasma level(during hospital stay, average of 1 week)
  • IL-6 plasma level(during hospital stay, average of 1 week)
  • Brain-derived neurotrophic factor (BDNF) plasma level(during hospital stay, average of 1 week)

Study Sites (1)

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