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The Impact of Electroencephalographic (EEG) Seizure Treatment in Neonatal Encephalopathy

Primary Purpose

Seizures, Encephalopathy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EEG monitoring and treatment of EEG seizures
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Seizures focused on measuring Neonatal Seizures, Neonatal encephalopathy

Eligibility Criteria

1 Hour - 72 Hours (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Term or near term infants ≥ 36 weeks gestation admitted to the neonatal intensive care unit
  • ≤ 72 hours of age
  • Screening for the "at risk" infant by the clinical team to include any one of the following:

    • Apgar score <5 at 5 min
    • Cord blood or postnatal gas with pH <7.0 or BE > -12
    • Need for respiratory support at 10 min of life
    • Suspected or definite seizures
    • Encephalopathy defined by recognition of altered neurological behavior
  • Infants identified in the above screen will be examined by the research team and will be eligible if they satisfy at least one of the following:

    • Moderate-severe neonatal encephalopathy (3 out of 6 criteria)
    • Suspected or definite neonatal seizures

Exclusion criteria:

  • Infants < 36 weeks gestation
  • > 72 hours of age
  • Infants with congenital anomalies of the central nervous system
  • Moribund infants for whom no further aggressive treatment is planned
  • Metabolic disorders or documented CNS infection
  • Neuro-muscular blockade

Sites / Locations

  • St. Louis Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

EEG seizure treatment group

Clinical Seizure treatment Group

Arm Description

EEG data available to physicians. Treatment based on EEG seizures. Treatment will be dictated by the detailed treatment protocol. Standard antiepileptic medications will be used.

Seizure treatment in this group will be based on standard care - treating clinical seizures only. While EEG data will be collected in this group, the data will not be available to the treating physicians. A one-hour EEG report will be available to the treating team. Continuous EEG monitoring and treatment will only be allowed if the initial EEG shows status.

Outcomes

Primary Outcome Measures

Seizure burden
Presence of a single combined event: death in the first two years of life or moderate or severe disability at 18-24 months

Secondary Outcome Measures

Time to seizure cessation
Number, duration of anticonvulsants used and cumulative dose
EEG background state
Time to all per oral feeding
Duration of hospital stay
MRI measures from the Day #7-10 MRI in survivors

Full Information

First Posted
December 8, 2009
Last Updated
December 8, 2015
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT01027715
Brief Title
The Impact of Electroencephalographic (EEG) Seizure Treatment in Neonatal Encephalopathy
Official Title
The Impact of Electroencephalographic (EEG) Seizure Treatment in Near Term ≥ 36 Weeks Gestation and Term Infants With Neonatal Encephalopathy
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a prospective, randomized, single-center pilot trial of term and near term (≥ 36 weeks gestation) infants with encephalopathy or seizures comparing a "EEG Seizure Treatment Group" or ESG with a "Clinical Seizure Treatment Group" or CSG. The investigators hypothesize that the accurate detection and treatment of EEG seizures will decrease the seizure burden and improve outcomes in newborn infants with seizures and/or hypoxic-ischemic encephalopathy (HIE).
Detailed Description
This is a prospective, randomized, pilot trial of term and near term (≥ 36 weeks gestation) infants with encephalopathy or seizures comparing a "EEG Seizure Treatment Group" or ESG with a "Clinical Seizure Treatment Group" or CSG. Eligibility is based on clinical criteria for moderate/severe encephalopathy or seizures. We will recruit near term or term infants (≥ 36 weeks gestation) with a diagnosis of seizures or encephalopathy admitted to the neonatal intensive care unit (NICU) at St. Louis Children's Hospital within the first 72 hours of life. Infants will be randomized into an EEG Seizure Treatment Group (ESG) or a Clinical Seizure Treatment Group (CSG) (n=20 in each group). Patients in both groups will have EEG monitoring. While treating physicians will have access to EEG data in the ESG, no EEG data in the CSG will be available to the clinician for treatment of seizures. AED treatment will be initiated/escalated using stringent EEG seizure criteria (EST) or clinical criteria (CST) with the goal being seizure cessation. The specific AED, dosage, and duration of treatment is standardized in both groups. Monitoring will continue for a period of upto 96 hours in both arms. Other than the anticonvulsant drugs, treatment thresholds and dosing schedules, treatment in both arms will be at the discretion of the bedside physician.All infants will undergo an assessment of neuromotor disability and neurodevelopmental evaluation at 18 to 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Seizures, Encephalopathy
Keywords
Neonatal Seizures, Neonatal encephalopathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EEG seizure treatment group
Arm Type
Experimental
Arm Description
EEG data available to physicians. Treatment based on EEG seizures. Treatment will be dictated by the detailed treatment protocol. Standard antiepileptic medications will be used.
Arm Title
Clinical Seizure treatment Group
Arm Type
No Intervention
Arm Description
Seizure treatment in this group will be based on standard care - treating clinical seizures only. While EEG data will be collected in this group, the data will not be available to the treating physicians. A one-hour EEG report will be available to the treating team. Continuous EEG monitoring and treatment will only be allowed if the initial EEG shows status.
Intervention Type
Other
Intervention Name(s)
EEG monitoring and treatment of EEG seizures
Other Intervention Name(s)
EEG monitoring, Anti-epileptic drugs
Intervention Description
Seizures will prompt treatment with loading doses of phenobarbital (20mg/kg), fosphenytoin (20mg/kg),and midazolam (0.05mg/kg bolus and .15mg/kg/hr infusion tapered over 48 hours)in that order for persisting seizures.
Primary Outcome Measure Information:
Title
Seizure burden
Time Frame
2 to 3 years
Title
Presence of a single combined event: death in the first two years of life or moderate or severe disability at 18-24 months
Time Frame
first two years of life; 18-24 months
Secondary Outcome Measure Information:
Title
Time to seizure cessation
Time Frame
2 to 3 years
Title
Number, duration of anticonvulsants used and cumulative dose
Time Frame
2 to 3 years
Title
EEG background state
Time Frame
2 to 3 years
Title
Time to all per oral feeding
Time Frame
2 to 3 years
Title
Duration of hospital stay
Time Frame
2 to 3 years
Title
MRI measures from the Day #7-10 MRI in survivors
Time Frame
2 to 3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Hour
Maximum Age & Unit of Time
72 Hours
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Term or near term infants ≥ 36 weeks gestation admitted to the neonatal intensive care unit ≤ 72 hours of age Screening for the "at risk" infant by the clinical team to include any one of the following: Apgar score <5 at 5 min Cord blood or postnatal gas with pH <7.0 or BE > -12 Need for respiratory support at 10 min of life Suspected or definite seizures Encephalopathy defined by recognition of altered neurological behavior Infants identified in the above screen will be examined by the research team and will be eligible if they satisfy at least one of the following: Moderate-severe neonatal encephalopathy (3 out of 6 criteria) Suspected or definite neonatal seizures Exclusion criteria: Infants < 36 weeks gestation > 72 hours of age Infants with congenital anomalies of the central nervous system Moribund infants for whom no further aggressive treatment is planned Metabolic disorders or documented CNS infection Neuro-muscular blockade
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amit Mathur
Organizational Affiliation
Washington University in Saint Louis
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Louis Children's Hospital
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26482675
Citation
Srinivasakumar P, Zempel J, Trivedi S, Wallendorf M, Rao R, Smith B, Inder T, Mathur AM. Treating EEG Seizures in Hypoxic Ischemic Encephalopathy: A Randomized Controlled Trial. Pediatrics. 2015 Nov;136(5):e1302-9. doi: 10.1542/peds.2014-3777. Epub 2015 Oct 19.
Results Reference
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The Impact of Electroencephalographic (EEG) Seizure Treatment in Neonatal Encephalopathy

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