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Prognosis in Patients With Guillain-Barre Syndrome

Recruiting
Conditions
Guillain-Barre Syndrome
Registration Number
NCT06032741
Lead Sponsor
First Affiliated Hospital of Wenzhou Medical University
Brief Summary

The goal of this observational study is to explore significant indicators to predict the early prognosis and late prognosis in patients with Guillain-Barre syndrome.

Detailed Description

This is a multicenter study(approximately three) with over 450 subjects.Clinical data were collected by consulting the patient's electronic history. The data included demographic information, blood biochemical markers, clinical characteristics and electromyography. All participants provided their written informed consent to participate in this study.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
450
Inclusion Criteria
  • patients fulfilled clinical, biological, and electrophysiology criteria for Guillain-barre syndrome.
Exclusion Criteria
  • nonidiopathic Guillain-barre syndrome and Miller Fisher syndrome

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the severity of Guillain-barre syndromebaseline, at 1 week, at 26 weeks

The Guillain-Barre syndrome disability score is a wide scale for the severity of Guillain-Barre syndrome (0, optimal health; 1, minor symptoms, able to run; 2, able to walk unaided 10 m, unable to run; 3, able to walk 10 m across an open space with help; 4 bedridden or wheelchair users; 5, require assisted ventilation; 6, dead)(deceased).The higher the score, the worse the prognosis.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

First Affiliated Hospital of Wenzhou Medical University

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Wenzhou, Zhejiang, China

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