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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06032741
Other study ID # GBS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2, 2013
Est. completion date January 31, 2025

Study information

Verified date December 2022
Source First Affiliated Hospital of Wenzhou Medical University
Contact Binbin Deng
Phone dbinbin@aliyun.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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 information / eligibility

Status Recruiting
Enrollment 450
Est. completion date January 31, 2025
Est. primary completion date December 1, 2022
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility 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


Related Conditions & MeSH terms


Locations

Country Name City State
China First Affiliated Hospital of Wenzhou Medical University Wenzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
First Affiliated Hospital of Wenzhou Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary the severity of Guillain-barre syndrome 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. baseline, at 1 week, at 26 weeks
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