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A prospective cohort study of patients with Guillain-Barré syndrome

A prospective cohort study of patients with Guillain-Barré syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108315
Enrollment
Unknown
Registered
2025-08-28
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Guillain-Barré syndrome

Interventions

GBS group:none

Sponsors

First hospital of shanxi medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Provide signed and dated informed consent; 2. Male or female, age >= 18 years; 3. Meet the diagnostic criteria for GBS; 4. Drug treatment started within 14 days of onset (calculated as limb weakness).

Exclusion criteria

Exclusion criteria: 1. Previous use of egamod, IVIg, plasmapheresis, rituximab, immunosuppressants (e.g., azathioprine, cyclosporine, mycophenolate mofetil, tacrolimus, prednisone, etc.) within 28 days prior to treatment with egarmod or IVIg; 2. Patients have evidence supporting the diagnosis of other peripheral neuropathy; 3. Have serious comorbidities affecting functional scores, such as malignant tumors, severe cardiovascular disease, severe chronic obstructive pulmonary disease, etc

Design outcomes

Primary

MeasureTime frame
Guillain-Barré Syndrome Disability Scale;

Secondary

MeasureTime frame
INCAT Disability Scale;I-RODS Scale;Grip strength;MRC sum scores;

Countries

China

Contacts

Public ContactWei zhang

First hospital of shanxi medical university

1115125635@qq.com+86 177 1311 1510

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026