None listed
Conditions
Brief summary
To examine the effectiveness and tolerability of Intravenous Levetiracetam in the acute seizure setting
Interventions
Intravenous Levetiracetam will be administered in case of acute seizure (1000 mg over 5 minutes), for 1 dose only. Subjects will be observed and followed-up for the next 24 hrs following intravenous levetiracetam injection. Electroencephalographic recordings will be reviewed and subjects will be asked about adverse effects at 1, 12 and 24 hrs after intravenous administration of the agent.
Sponsors
Prof. David C. Reutens
Study design
Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Epilepsy patients admitted for pre-surgical work-up at Monash Medical Centre with occurrence of acute seizures during epilepsy monitoring
Exclusion criteria
Women who are pregnanat or are considering pregnancy, lactation, moderate to severe renal dysfunction
Outcome results
None listed