Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE1/PHASE2
INTERVENTIONAL
2023-01-11
2024-12-13
Brief Summary
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Detailed Description
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GAD65 antibodies have been identified in a subset of patients with drug resistant focal epilepsy and limbic encephalitis. While it has not been definitively determined that these antibodies cause GAD65 inhibition and GABA depletion directly, diazepam, a common benzodiazepine, has been established as a mainstay of therapy for stiffperson's syndrome, a condition that is commonly associated with GAD65 antibody positivity. Given these observations, diazepam has been used by the investigators in a small number of patients with intractable epilepsy in the setting of GAD65 antibody positivity, with some encouraging anecdotal results with one patient being rendered seizure free for three years.
The purpose of this study is to generate prospective data on use of diazepam in patients with epilepsy related to high-titer GAD65 antibody positivity.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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GAD65 Associated Epilepsy
Subjects diagnosed with GAD65 associated epilepsy, serum high-titer GAD65 positivity, trialed and failed at least 2 anti-seizure medications, at least 4 seizures per month will be started on diazepam.
Diazepam
5 mg twice daily oral for 1 week and then increase to 10 mg twice daily oral
Interventions
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Diazepam
5 mg twice daily oral for 1 week and then increase to 10 mg twice daily oral
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Drug-resistant focal epilepsy, having failed 2 previous anti-seizure medications.
* Stable treatment for the 1 month prior to enrollment.
* Patients must be able to give informed consent or have an appropriate representative available to do.
Exclusion Criteria
* Already on another benzodiazepine.
* On a regularly scheduled opiate.
* Co-existing antibodies associated with seizures.
* Pregnancy or breast feeding.
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Kelsey M. Smith
Principal Investigator
Principal Investigators
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Kelsey Smith, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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21-007195
Identifier Type: -
Identifier Source: org_study_id
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