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Trial registered on ANZCTR
Registration number
ACTRN12608000293369
Ethics application status
Approved
Date submitted
30/05/2008
Date registered
12/06/2008
Date last updated
3/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Intravenous Levetiracetam in the Acute Management of Seizures
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Scientific title
Intravenous Levetiracetam in the Acute Management of Seizures in Epilepsy
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
acute seizures
3216
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Condition category
Condition code
Neurological
3380
3380
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0
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Epilepsy
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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.
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Intervention code [1]
2957
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Treatment: Drugs
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Comparator / control treatment
N/A
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Termination/Control of acute seizure after intravenous infusion of Levetiracetam 1000 mg over 5 minutes
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Assessment method [1]
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Timepoint [1]
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Rapid termination of seizure after giving the medication
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Secondary outcome [1]
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Decrease frequency of seizure occurrence and interictal spikes per hour
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Assessment method [1]
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Timepoint [1]
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24 hours following intravenous levetiracetam injection
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Eligibility
Key inclusion criteria
Epilepsy patients admitted for pre-surgical work-up at Monash Medical Centre with occurrence of acute seizures during epilepsy monitoring
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Women who are pregnanat or are considering pregnancy, lactation, moderate to severe renal dysfunction
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/06/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
20
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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UCB Pharma
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Address [1]
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Level 1 1155 Malvern Road Malvern Victoria 3144
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Prof. David C. Reutens
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Address
Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr. Pilita Valencia
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Address [1]
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Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country [1]
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Dr. Yong Chern Lee
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Address [1]
299
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Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country [1]
299
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Australia
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Other collaborator category [2]
308
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Individual
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Name [2]
308
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Dr. Simon Bower
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Address [2]
308
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Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country [2]
308
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Australia
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Other collaborator category [3]
309
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Individual
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Name [3]
309
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Dr. Udaya Seneviratne
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Address [3]
309
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Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country [3]
309
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
5469
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Southern Health Human Research Ethics Committee
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Ethics committee address [1]
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Level 4 Main Block Monash Medical Centre 246 Clayton Road Clayton Victoria 3168
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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20/12/2007
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Approval date [1]
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18/01/2008
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Ethics approval number [1]
5469
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07203C
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Summary
Brief summary
To examine the effectiveness and tolerability of Intravenous Levetiracetam in the acute seizure setting
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
28635
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Prof. David C. Reutens
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Address
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Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country
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Australia
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Phone
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+61395942240
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Fax
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+61395946241
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Email
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[email protected]
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Contact person for scientific queries
Name
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Prof. David C. Reutens
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Address
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Department of Neurosciences
Level 5 Block E
Monash Medical Centre
246 Clayton Road
Clayton Victoria 3168
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Country
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Australia
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Phone
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+61395942240
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Fax
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+61395946241
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF