Seizure Disorder Clinical Trial
Official title:
IVIG Treatment for Refractory Immune-Related Adult Epilepsy
The purpose of the initial screening study is to find out if immune problems are an
unrecognized cause of epilepsy in some patients. This study consists of a single blood
sample, which will be tested for possible immune abnormalities. If enough patients are found
who show immune abnormalities, those patients who are still having uncontrolled seizures
will be invited to participate in a study of immune treatment with a compound called
intravenous immunoglobulin (IVIG).
The study hypothesis is that a significant proportion of the young-onset, refractory,
image-negative, partial-onset epilepsy population have an underlying autoimmune disorder,
and many of these patients will respond to immune therapies, including IVIG.
At present, the importance of immune abnormalities in causing epilepsy, and the proper
treatment when they are found, are both poorly understood. The investigators hope that this
study will help us understand the cause of some cases that are difficult to treat.
The study is divided into two phases:
Phase I: The investigators will screen for evidence of neuronal nuclear, cytoplasmic, and
cell surface autoantibodies in our population of new onset refractory, imaging-negative
young adult epilepsy patients. This part of the study involves obtaining a single blood
sample, equal to about 2 teaspoons.
Phase 2: If a sufficient number of cases are identified, a double-blind crossover study of
IVIG treatment will be performed in these patients.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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