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Clinical Trial Summary

The purpose of this study is to determine whether intravenous immunoglobulin (IVIG) treatment reduces significantly the number of epileptic seizures in cases of autoimmune epileptic seizures.


Clinical Trial Description

The purpose of this study is to determine if intravenous immunoglobulin (IVIG) treatment significantly reduces the number of epileptic seizures in cases of autoimmune epilepsy. Potential participants will be screened at an outpatient neurology clinic visit appointment. Interested qualified potential participants will be consented and offered participation in this trial. Once consent has been obtained, and it is determined that the participant meets all inclusion criteria, the participant will be randomized to either IVIG or placebo treatment for the next 5 weeks. Participants will return to Mayo Clinic for an evaluation. Those participants that received the placebo for 5 weeks will be given IVIG in an open label fashion for 5 weeks (week 7-11) then return to Mayo Clinic for evaluation. All participants will receive monthly phone calls after they complete the IVIG treatment for a period of 1 year from the end of IVIG 5 week course. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02697292
Study type Interventional
Source Mayo Clinic
Contact
Status Terminated
Phase Phase 3
Start date February 2016
Completion date December 3, 2018

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05627661 - Wearable Devices to Monitor Seizures in Autoimmune Epilepsy N/A