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Efficacy of Levetiracetam in Control of Neonatal Seizures Guided by an EEG

Primary Purpose

Neonatal Seizures

Status
Unknown status
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Levetiracetam
Phenobarbital
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neonatal Seizures focused on measuring EEG with Periodic Abnormalities, Levetiracetam, Phenobarbitone, neonatal seizures, Neurodevelopmental Abnormality

Eligibility Criteria

1 Hour - 30 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All full term neonates experiencing seizures due to; post-hypoxic or post-ischemic encephalopathy, intracerebral hemorrhage, cerebral infection, inborn errors of metabolism or malformations of cortical development

Exclusion Criteria:

  • Preterm neonates
  • Full term neonates with seizures due to metabolic derangements (hypoglycemia, hypocalcemia or hypomagnesemia)
  • Full term neonates with impaired renal functions.

Sites / Locations

  • Cairo University Children's Hospital (Abulreesh)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Levetiracetam

Phenobarbital

Arm Description

Levetiracetam given in oral form via oro-gastric tube, first a bolus dose 40-50mg/kg then maintenance dose 10-30 mg/kg/day divided every 12 hours. Duration: until seizure free

Phenobarbital given in IV form, loading dose 20mg/kg that can be repeated after a 20 minute interval not to exceed 40mg/kg then maintenance dose 2-4 mg/kg/day divided every 12 hours. Duration: until seizure free

Outcomes

Primary Outcome Measures

Efficacy of levetiracetam in control of neonatal seizures as a first line versus phenobarbital through assessment of seizure burden.
Number of seizures before and after levetiracetam administration in comparison to phenobarbital.
Efficacy of levetiracetam in rapid control of neonatal seizures compared to phenobarbital.
Number of hours taken to achieve seizure freedom after administration of levetiracetam versus phenobarbital.

Secondary Outcome Measures

Dose escalation data about levetiracetam through studying the efficacy of further dose administration in non responders.
Number of originally non responder participants who achieved seizure control with higher doses of levetiracetam.
Adequacy of levetiracetam as a single agent antiepileptic drug in control of neonatal seizures.
Number of participants who require addition of second line antiepileptic drug to control seizures after levetiracetam versus phenobarbital use.
Accuracy of amplitude integrated EEG monitoring in detecting neonatal seizures before and after antiepileptic drug use.
Number of seizures detected by aEEG before and after antiepileptic drug use.
Effect of levetiracetam on aEEG background activity of participants.
Number of participants with normalization of background activity after administration of levetiracetam versus phenobarbital.
The short term clinical outcome of patients with neonatal seizures after treatment with levetiracetam.
Neurodevelopmental assessment through detecting presence of following milestones: Head control Social smile Visual fixation and pursuit Turning towards sounds
The short term electroencephalographic outcome of patients with neonatal seizures after treatment with levetiracetam
Number of participants with presence of epileptogenic activity on follow up electroencephalogram.

Full Information

First Posted
February 22, 2017
Last Updated
April 5, 2017
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT03107507
Brief Title
Efficacy of Levetiracetam in Control of Neonatal Seizures Guided by an EEG
Official Title
Efficacy of Levetiracetam in Control of Neonatal Seizures
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 25, 2017 (Actual)
Primary Completion Date
October 30, 2017 (Anticipated)
Study Completion Date
December 30, 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Over the last three decades, several tools have been developed to enhance the detection and treatment of neonatal seizures. Regarding treatment, phenobarbital maintains is still used as a first-line therapy worldwide. However, newer anti-epileptic drugs (AED) s such as, levetiracetam, bumetanide, and topiramate are increasingly being applied to the neonatal population, offering the potential for seizure treatment with a significantly better side-effect profile. Levetiracetam is a very promising medication for the treatment of neonatal seizures. It has been in clinical use for almost a decade in adults and older children with good efficacy, an excellent safety profile and near ideal pharmacokinetic characteristics. It has been approved and used for treatment of seizures in infants starting one month of age since 2012. The investigators are comparing the efficacy of levetiracetam to that of phenobarbital as a first-line drug in control of neonatal seizures. The investigators monitor the efficacy through assessment of frequency of seizures before and after drug administration, amplitude integrated EEG changes in background activity and seizure frequency in participants, duration taken for participants to be seizure free and short term neurodevelopmental outcome and EEG at 3 months of age

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal Seizures
Keywords
EEG with Periodic Abnormalities, Levetiracetam, Phenobarbitone, neonatal seizures, Neurodevelopmental Abnormality

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Levetiracetam
Arm Type
Active Comparator
Arm Description
Levetiracetam given in oral form via oro-gastric tube, first a bolus dose 40-50mg/kg then maintenance dose 10-30 mg/kg/day divided every 12 hours. Duration: until seizure free
Arm Title
Phenobarbital
Arm Type
Active Comparator
Arm Description
Phenobarbital given in IV form, loading dose 20mg/kg that can be repeated after a 20 minute interval not to exceed 40mg/kg then maintenance dose 2-4 mg/kg/day divided every 12 hours. Duration: until seizure free
Intervention Type
Drug
Intervention Name(s)
Levetiracetam
Intervention Description
Given in a bolus dose first 50mg/kg as levetiracetam reaches a therapeutic serum level rapidly in 1.3 hours. Titration will not be attempted in our study to reach drug level rapidly and consequent rapid effective control of seizures. Maintenance dose is then given at a dose of 10 - 40mg/kg/day divided every 12 hours.
Intervention Type
Drug
Intervention Name(s)
Phenobarbital
Intervention Description
Phenobarbital is given intravenously in the form of a loading dose of 15mg/kg that can be repeated after a 20 minute interval not to exceed 30mg/kg then a maintenance dose 2-4 mg/kg/day divided every 12 hours.
Primary Outcome Measure Information:
Title
Efficacy of levetiracetam in control of neonatal seizures as a first line versus phenobarbital through assessment of seizure burden.
Description
Number of seizures before and after levetiracetam administration in comparison to phenobarbital.
Time Frame
72 hours
Title
Efficacy of levetiracetam in rapid control of neonatal seizures compared to phenobarbital.
Description
Number of hours taken to achieve seizure freedom after administration of levetiracetam versus phenobarbital.
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
Dose escalation data about levetiracetam through studying the efficacy of further dose administration in non responders.
Description
Number of originally non responder participants who achieved seizure control with higher doses of levetiracetam.
Time Frame
72 hours
Title
Adequacy of levetiracetam as a single agent antiepileptic drug in control of neonatal seizures.
Description
Number of participants who require addition of second line antiepileptic drug to control seizures after levetiracetam versus phenobarbital use.
Time Frame
30 days
Title
Accuracy of amplitude integrated EEG monitoring in detecting neonatal seizures before and after antiepileptic drug use.
Description
Number of seizures detected by aEEG before and after antiepileptic drug use.
Time Frame
48 hours
Title
Effect of levetiracetam on aEEG background activity of participants.
Description
Number of participants with normalization of background activity after administration of levetiracetam versus phenobarbital.
Time Frame
48 hours
Title
The short term clinical outcome of patients with neonatal seizures after treatment with levetiracetam.
Description
Neurodevelopmental assessment through detecting presence of following milestones: Head control Social smile Visual fixation and pursuit Turning towards sounds
Time Frame
3 months
Title
The short term electroencephalographic outcome of patients with neonatal seizures after treatment with levetiracetam
Description
Number of participants with presence of epileptogenic activity on follow up electroencephalogram.
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
To gather safety information on levetiracetam use in neonates
Description
By collecting data of renal and liver function tests 48-72 hours after treatment.
Time Frame
72 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Hour
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All full term neonates experiencing seizures due to; post-hypoxic or post-ischemic encephalopathy, intracerebral hemorrhage, cerebral infection, inborn errors of metabolism or malformations of cortical development Exclusion Criteria: Preterm neonates Full term neonates with seizures due to metabolic derangements (hypoglycemia, hypocalcemia or hypomagnesemia) Full term neonates with impaired renal functions.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yara S Shaheen, Msc
Phone
01227981313
Ext
002
Email
yarasalah.shaheen@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Aliaa A Ali, MD
Email
draliaaadel@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Omneya G Afify, MD
Organizational Affiliation
Cairo University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Iman F Iskander, MD
Organizational Affiliation
Cairo University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Aliaa A Ali, MD
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yara S Shaheen, MSc.
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Walaa Shaarany, MD
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cairo University Children's Hospital (Abulreesh)
City
Cairo Governorate
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yara Shaheen

12. IPD Sharing Statement

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Efficacy of Levetiracetam in Control of Neonatal Seizures Guided by an EEG

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