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Effectiveness of Combined Levetiracetam and Midazolam in Generalized Convulsive Status Epilepticus in Children

Primary Purpose

Status Epilepticus, Generalized Convulsive Status Epilepticus, Status Epilepticus, Generalized

Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Levetiracetam
Midazolam
Placebo
Sponsored by
Sohag University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Status Epilepticus focused on measuring Status epilepticus, Convulsions, Children, Seizures, Benzodiazepines, Midazolam, Levetiracetam

Eligibility Criteria

1 Month - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Generalized convulsive status epilepticus, which is clinically defined at the time of presentation as continuous, generalized, tonic-clonic seizure activity or ≥ 2 generalized tonic-clonic seizures without recovery of consciousness for more than 5 minutes.

Exclusion Criteria:

  • Failure to obtain informed consent.
  • Prior therapy with any anticonvulsant for the presenting episode of generalized convulsive status epilepticus.
  • Epileptic patients on levetiracetam therapy.
  • Known allergy or contraindications to any of the study drugs.
  • End-stage kidney disease.
  • Severe liver disease.
  • Cardiac diseases.
  • Hypoglycemia or hyperglycemia.
  • Inborn errors of metabolism.
  • Known mood/behavioral disorder.
  • Failure to obtain intravenous access in the first 5 minutes.
  • Cessation of seizures during the stabilization phase (0 - 5 minutes).
  • Traumatic brain injury

Sites / Locations

  • Department of Pediatrics - Sohag University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Study group

Control group

Arm Description

Children receiving levetiracetam + midazolam

Children receiving placebo + midazolam

Outcomes

Primary Outcome Measures

Cessation of seizures
Cessation of clinical seizures at 20 minutes timepoint (end of first therapy phase)

Secondary Outcome Measures

Need for repeating midazolam
Need for repeating midazolam during the first therapy phase (5 - 20 min)
Cessation of seizures
Cessation of clinical seizures at 40 minutes timepoint (end of second therapy phase).
Seizure control
24-hours seizure control (no visually observed recurrence of seizures after the end of second phase therapy with improved sensorium)
Hypotension
Occurrence of hypotension
Need for mechanical ventilation
Need for mechanical ventilation
Skin rash
Occurrence of skin rash
Agitation/aggression
Occurrence of agitation/aggression
Mortality
Occurrence of death

Full Information

First Posted
June 14, 2021
Last Updated
September 17, 2022
Sponsor
Sohag University
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1. Study Identification

Unique Protocol Identification Number
NCT04926844
Brief Title
Effectiveness of Combined Levetiracetam and Midazolam in Generalized Convulsive Status Epilepticus in Children
Official Title
Effectiveness of Combined Levetiracetam and Midazolam in Treatment of Generalized Convulsive Status Epilepticus in Children
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
June 20, 2021 (Actual)
Primary Completion Date
August 30, 2022 (Actual)
Study Completion Date
September 1, 2022 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Generalized status epilepticus is a common pediatric neurological emergency with significant mortality and morbidity. Benzodiazepines remain the first anticonvulsive line but benzo-diazepines don't control seizures in about 30% of cases. GCSE may be more rapidly stopped and controlled through combining another drug with benzodiazepines such as Levetiracetam, acting by different pathways. This study aims to evaluate the effectiveness of combined levetiracetam and midazolam in treatment of generalized convulsive status epilepticus in children.
Detailed Description
Generalized convulsive status epilepticus (GCSE) is a common pediatric neurological emergency with an annual incidence of up to 73 episodes per 100,000 children and is associated with mortality in 2.7% of cases and overall morbidity in 10% - 20% of cases, including hemodynamic instability and long-term neurological impairments. The management of GCSE in children starts with emergency measures (stabilization phase) with monitoring and laboratory testing in the first 5 minutes. Benzodiazepines are used as first-line anticonvulsants for GCSE that persists for more than 5 minutes. However, studies have shown that benzo-diazepines don't control GCSE in about 30% of patients. GCSE may be more rapidly stopped and controlled through combining another drug with benzodiazepines, acting by different pathways. Levetiracetam is a recent broad-spectrum antiepileptic drug with a relatively high safety profile. The effectiveness of intravenous levetiracetam has been demonstrated as a second-line anticonvulsant in GCSE. In this study, we aim to evaluate the effectiveness and safety of levetiracetam plus midazolam versus midazolam alone as first-line therapy of GCSE in children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Status Epilepticus, Generalized Convulsive Status Epilepticus, Status Epilepticus, Generalized, Status Epilepticus, Generalized Convulsive
Keywords
Status epilepticus, Convulsions, Children, Seizures, Benzodiazepines, Midazolam, Levetiracetam

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Two groups of children with continuing seizures after stabilization phase (5 minutes): Study group; will receive intravenous levetiracetam 60 mg/kg (max 4500 mg) over 5 minutes (diluted with isotonic saline to a concentration of 50 mg/ml). Control group will receive intravenous isotonic saline (as a placebo) in the same way. At the same time, both groups will receive intravenous midazolam 0.2 mg/kg (maximum 10 mg) over 2 minutes.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Each enrolled child will be assigned a unique identification number. Pharmacy will fill the active and placebo preparations in similar containers with sealed code for identification. Participants' families, treating clinicians, and investigators will be unaware of group assignment and drug/placebo therapy.
Allocation
Randomized
Enrollment
144 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study group
Arm Type
Experimental
Arm Description
Children receiving levetiracetam + midazolam
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Children receiving placebo + midazolam
Intervention Type
Drug
Intervention Name(s)
Levetiracetam
Other Intervention Name(s)
Keppra, Tiratam
Intervention Description
Intravenous levetiracetam 60 mg/kg (max 4500 mg) over 5 minutes (diluted with isotonic saline to a concentration of 50 mg/ml).
Intervention Type
Drug
Intervention Name(s)
Midazolam
Intervention Description
Intravenous midazolam 0.2 mg/kg (maximum 10 mg) over 2 minutes
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Intravenous isotonic saline (1.2 ml/kg) over 5 minutes
Primary Outcome Measure Information:
Title
Cessation of seizures
Description
Cessation of clinical seizures at 20 minutes timepoint (end of first therapy phase)
Time Frame
20 minutes
Secondary Outcome Measure Information:
Title
Need for repeating midazolam
Description
Need for repeating midazolam during the first therapy phase (5 - 20 min)
Time Frame
20 minutes
Title
Cessation of seizures
Description
Cessation of clinical seizures at 40 minutes timepoint (end of second therapy phase).
Time Frame
40 minutes
Title
Seizure control
Description
24-hours seizure control (no visually observed recurrence of seizures after the end of second phase therapy with improved sensorium)
Time Frame
24 hours
Title
Hypotension
Description
Occurrence of hypotension
Time Frame
24 hours
Title
Need for mechanical ventilation
Description
Need for mechanical ventilation
Time Frame
24 hours
Title
Skin rash
Description
Occurrence of skin rash
Time Frame
24 hours
Title
Agitation/aggression
Description
Occurrence of agitation/aggression
Time Frame
24 hours
Title
Mortality
Description
Occurrence of death
Time Frame
24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Generalized convulsive status epilepticus, which is clinically defined at the time of presentation as continuous, generalized, tonic-clonic seizure activity or ≥ 2 generalized tonic-clonic seizures without recovery of consciousness for more than 5 minutes. Exclusion Criteria: Failure to obtain informed consent. Prior therapy with any anticonvulsant for the presenting episode of generalized convulsive status epilepticus. Epileptic patients on levetiracetam therapy. Known allergy or contraindications to any of the study drugs. End-stage kidney disease. Severe liver disease. Cardiac diseases. Hypoglycemia or hyperglycemia. Inborn errors of metabolism. Known mood/behavioral disorder. Failure to obtain intravenous access in the first 5 minutes. Cessation of seizures during the stabilization phase (0 - 5 minutes). Traumatic brain injury
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abdelrahim A Sadek, MD, PhD
Organizational Affiliation
Sohag University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Pediatrics - Sohag University Hospital
City
Sohag
ZIP/Postal Code
82524
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Unidentified individual patients' data will be available on resonable request after publication
IPD Sharing Time Frame
After publication for 3 years
IPD Sharing Access Criteria
Contact the principal investigator
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Effectiveness of Combined Levetiracetam and Midazolam in Generalized Convulsive Status Epilepticus in Children

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