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Efficacy of Intravenous Gamma Globulin on Guillain-Barre Syndrome

N

Ning Wang, MD., PhD.

Status

Enrolling

Conditions

Guillain-barre Syndrome

Study type

Observational

Funder types

Other

Identifiers

NCT04303962
MRCTA,ECFAH of FMU[2019]217

Details and patient eligibility

About

Guillain-barre syndrome (GBS) is an acute immune-mediated polyneuropathy. Intravenous Gamma globulin is an effective therapy.Although high doses of gamma globulin are clinically effective, the patient's recovery and clinical prognosis vary. The establishment of a cohort study on the therapeutic effect of gamma globulin in Guillain-barre Syndrome is beneficial to the diagnosis of the disease and to the understanding of the natural course of the disease and the efficacy of drug treatment.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Meet the Brighton Guillain-Barre Syndrome diagnosis criteria in 2014;

  2. Age ≥18;

  3. Patients with AIDP, AMAN and AMSAN;

  4. IVIG was treated within 2 weeks of onset; 6. GBS disability scale>2; 6. Cooperate with patients who were followed up for 180 days and sign the informed consent;

Exclusion criteria

  1. Age <18;
  2. Pregnant or nursing women;
  3. Patients with Chronic inflammatory demyelinating multiple peripheral neuropathy;
  4. Combined with other types of immune system diseases;
  5. Accept drugs that affect the function of the immune system within 5 or 3 months;
  6. Concomitant neoplastic diseases.
  7. The patient or guardian refused to sign the informed consent.

Trial contacts and locations

1

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Central trial contact

Ying Fu, PhD; Zhu MD Jiitng, PhD

Data sourced from clinicaltrials.gov

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