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Sponsors and Collaborators: |
FDA Office of Orphan Products Development Emory University |
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Information provided by: | FDA Office of Orphan Products Development |
ClinicalTrials.gov Identifier: | NCT00004833 |
OBJECTIVES:
I. Compare the efficacy of plasmapheresis and human immunoglobulin infusion in minimizing morbidity and augmenting the pace of recovery in children with Guillain-Barre syndrome.
II. Compare the potential risks, in terms of treatment related side effects and adverse clinical outcome, between these two treatment modalities.
Condition | Intervention |
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Guillain-Barre Syndrome |
Drug: Immune globulin |
Study Type: | Interventional |
Study Design: | Treatment, Randomized |
Estimated Enrollment: | 170 |
Study Start Date: | July 1995 |
PROTOCOL OUTLINE:
This is a randomized, multicenter study.
Patients are randomized to receive either human immunoglobulin infusion (IVIg) (arm I) or plasmapheresis (arm II).
Arm I patients receive liquid heat-treated IVIg for 4 days starting on day 1 and then another single infusion of IVIg on day 7, 8, or 9.
Arm II patients receive serial plasmapheresis treatments. The first exchange is given on day 1 and the remaining exchanges are given over the next 5-10 days.
Patients are followed at weeks 1, 2, 3, 4, 8, 12, and 24.
Ages Eligible for Study: | up to 17 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
Guillain-Barre syndrome (GBS): Progressive weakness of two or more limbs; Absence or reduced tendon reflexes; No atypical symptoms of GBS (e.g., Miller-Fisher variant); No pure sensory neuropathy; No prior history of GBS
Disability at least grade 3 according to Guillain-Barre Study Group grading scale (unable to walk 5 meters without assistance); Must not have improvement of one or more disability grades prior to randomization in this study
No paresthesias, numbness, or weakness that began more than 14 days before randomization in this study
No CNS involvement
--Prior/Concurrent Therapy--
Biologic therapy: No prior treatment with plasmapheresis or infusion of human immunoglobulin (IVIg)
Endocrine therapy: No concurrent corticosteroids or other immunosuppressants (except for concurrent medical conditions, e.g., asthma)
Radiotherapy: Not specified
Surgery: Not specified
Other: No concurrent mechanical ventilation
--Patient Characteristics--
Age: Under 18 but with at least 3 months of independent walking
Hematopoietic: Cerebrospinal fluid leukocyte count less than 50/mm3
Hepatic: No liver failure
Renal: No kidney failure
Neurological: No other major neurologic diseases, other neuromuscular disorders, or cerebral palsy
Other: HIV negative; No contraindications to plasmapheresis or IVIg; No severe uncontrolled infection; No known IgA hypersensitivity; No other preexisting disease that would interfere with assessment of disability grades; No other causes of acquired weakness (e.g., poliomyelitis, botulism, or other etiologies); No diabetes; Not pregnant
Study ID Numbers: | 199/13444, EUSM-076-97, EUSM-FDR001265 |
Study First Received: | February 24, 2000 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00004833 |
Health Authority: | United States: Federal Government |
Guillain-Barre syndrome demyelinating neuropathy neurologic and psychiatric disorders rare disease |
Autoimmune Diseases Demyelinating Diseases Polyradiculoneuropathy Rare Diseases Polyneuropathies Demyelinating diseases Antibodies Neuromuscular Diseases |
Guillain-Barre syndrome Acute idiopathic polyneuritis Guillain-Barre Syndrome Mental Disorders Peripheral Nervous System Diseases Autoimmune Diseases of the Nervous System Immunoglobulins |
Pathologic Processes Disease Immunologic Factors Immune System Diseases |
Syndrome Physiological Effects of Drugs Nervous System Diseases Pharmacologic Actions |