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International GBS Outcome Study.

Recruiting
Conditions
Guillain-Barré syndrome
Registration Number
NL-OMON22932
Lead Sponsor
Erasmus Medical Center
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
1000
Inclusion Criteria

Criteria for inclusion of patients in the IGOS:

1. Fulfil the diagnostic criteria for GBS of the National Institute of Neurological Disorders and Stroke (NINDS). In addition all patients with Miller Fisher syndrome (MFS) and other variants of GBS, including overlap syndromes can be included, for which additional diagnostic criteria will be provided;

Exclusion Criteria

To limit selection bias as much as possible there are no exclusion criteria to be included in IGOS.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary clinical outcomes in IGOS are disability (GBS disability score and R-ODS), weakness (MRC sumscore), Limitations (ONLS), Fatigue (FSS) and quality of life (EuroQoL) during a follow-up of one year.
Secondary Outcome Measures
NameTimeMethod
Secondary outcomes in IGOS are these same items at two and three year after diagnosis, and the complications caused by GBS.
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