Antiepileptic Drugs and Vascular Risk Markers
Subarachnoid Hemorrhage
About this trial
This is an interventional treatment trial for Subarachnoid Hemorrhage focused on measuring vascular risk, lipid fractions, lipoprotein(a), C-reactive protein, subarachnoid hemorrhage, antiepileptic drug, randomized, seizure, cholesterol
Eligibility Criteria
Inclusion Criteria:
- Acute subarachnoid hemorrhage, Hunt-Hess Grades I-IV
- Within 48 hours of admission
Exclusion Criteria:
- Grade V subarachnoid hemorrhage
- Being treated with a lipid-lowering agent
- Contraindication to phenytoin, valproate, or levetiracetam (e.g. history of allergy to one of these agents)
- Contraindication to receiving no antiepileptic drug treatment (e.g. history of pre-existing epilepsy, seizure activity on admission EEG)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Active Comparator
Active Comparator
No Intervention
1
2
3
4
Participants randomized to Group 1 will receive phenytoin (PHT) at 5 mg/kg/day in 2 divided doses.
Participants randomized to Group 2 will receive valproate (VPA) at 15 mg/kg/day in 3 divided doses or in a once-daily extended release formulation.
Participants randomized to Group 3 will receive levetiracetam (LEV) 1000-1500 mg/day in 2 divided doses.
Participants randomized to Group 4 will receive no drug intervention.