Seizure Prevention in Traumatic Brain Injury With Levetiracetam and Lacosamide
Start Date
4/18/2025
Completion Date
4/1/2027
Summary
The purpose of this study is to assess the incidence of early post-traumatic seizures. The study will also assess the benefit of lacosamide compared to levetiracetam in regards to agitation and behavioral adverse effects in patients with traumatic brain injury requiring seizure prophylaxis.
Detailed Description
This is a prospective randomized controlled trial of patients with TBI requiring seizure prophylaxis to prevent early and late posttraumatic seizures. Patients will be identified and randomized as soon as possible, within 24 hours, from injury and started on seizure prophylaxis if they meet the predefined inclusion and exclusion criteria. Patients randomized to the levetiracetam group will receive levetiracetam 1000 mg intravenously or by mouth twice daily for a total of 7 days. Patients randomized to the lacosamide group will receive lacosamide 200 mg intravenously or by mouth twice daily for a total of 7 days.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
levetiracetam
lacosamide
Conditions
Locations
Wake Forest University Health Sciences
Winston-Salem, North Carolina 27157
United States