Barnes-jewish Hospital
St Louis, Missouri, 63110, United States
NCT Number: NCT01137110
Our primary objective is to compare two treatment options for prevention of seizures following a subarachnoid hemorrhage and determine if a short-course regimen of levetiracetam is as efficacious in the prevention of in-hospital seizures when compared to an extended course.
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Notify Me18 year–99 year
All sexes
Interventional
Not applicable
St Louis, Missouri, 63110, United States
This is a prospective, single-center, randomized, controlled trial. Patients admitted with spontaneous SAH (and meet enrollment criteria) will be randomized to either levetiracetam 1000 mg twice daily for 3 days or levetiracetam 1000mg twice daily until hospital discharge.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Levetiracetam 1000mg BID x 3 days for prophylaxis
Levetiracetam 1000mg BID for length of hospital stay for prophylaxis
Time frame: from hospital admission to hospital discharge
from admission to In-hospital seizures after aSAH
Washington University School of Medicine
Other
Comparison of Short Duration Levetiracetam to Extended Course Levetiracetam for Seizure Prophylaxis Following Subarachnoid Hemorrhage
Acronym: DOPAST
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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