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NCT Number: NCT07046611

Ketamine and Levetiracetam as Second-line Antiseizure Medication for Status Epilepticus in Children

About 40% of children with generalized convulsive status epilepticus (GCSE) are not terminated by first-line benzodiazepines (BDZs), and approximately 50% of BDZ-refractory GCSE are not controlled by second-line antiseizure medications. This study investigates the efficacy of ketamine-levetiracetam combination vs. levetiracetam alone for treating children with BDZ-refractory GCSE.

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Key information

Age range

1 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Department of Pediatrics at Sohag University Hospital

Sohag, 82524, Egypt

Location status: Recruiting

Location contact

Abdelrahim A Sadek, MD, PhD

CONTACT

[email protected]

About this study

Generalized convulsive status epilepticus (GCSE) is the most common pediatric neurological emergency. Benzodiazepines (BDZs) are the recommended first-line anti-seizure medication (ASM) for GCSE, but they fail to halt seizures in about 40% of cases. Moreover, approximately 50% of BDZ-refractory GCSE are not terminated by second-line ASMs, including levetiracetam, valproate, and phenytoin. Continuous GCSE for a longer duration is associated with progressive brain injury and a higher risk of mortality, epilepsy, and permanent neurodevelopmental impairment. Therefore, early control of GCSE is pivotal for improving patients' outcomes.

A potential approach for early control of GCSE is the use of early ASM polytherapy. Ketamine is a promising option to be combined with standard ASMs for more rapid control of seizures. Ketamine has been used for decades for pediatric procedural analgosedation due to its excellent safety profile and wide therapeutic index. Ketamine works as a noncompetitive antagonist for N-methyl-D-aspartate (NMDA) receptors, which are progressively upregulated by way of receptor trafficking during ongoing seizure activity. Ketamine administration is associated with termination or attenuation of refractory SE (RSE) and super-refractory SE (SRSE). Multiple observational studies have reported the efficacy of ketamine in the pre-hospital emergency treatment of BZD-refractory status epilepticus. Furthermore, the recently published Ket-Mid study demonstrated that the ketamine-midazolam combination was more effective than midazolam alone in the initial treatment of pediatric GCSE. However, the value of combining ketamine with levetiracetam for the treatment of BZD-refractory status epilepticus has not been well investigated.

The present study (Ketamine and Levetiracetam as Second-line antiseizure medication for Status Epilepticus in Children, KLaSSEC) aims to investigate the efficacy of ketamine-levetiracetam combination vs. levetiracetam alone for treating children with BDZ-refractory GCSE. The findings could help earlier control of seizures and better clinical outcomes for children with status epilepticus

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age from 1 year to 16 years.
  • Generalized convulsive status epilepticus (GCSE), defined as clinically observed generalized tonic-clonic convulsions that continue or recur without complete regaining of consciousness in between for longer than 5 minutes.
  • Benzodiazepine-refractory, defined as continuous or recurrent GCSE in the emergency room after receiving an adequate benzodiazepine dose, with the last dose administered within 5 to 30 minutes.

Exclusion criteria

  • Failure to obtain informed consent.
  • Prior treatment with antiseizure medication or anticonvulsant sedatives other than benzodiazepines for the presenting GCSE episode.
  • Endotracheal intubation before enrollment.
  • Acute traumatic brain injury.
  • Cardiac arrest/post-anoxic seizures
  • Hypoglycemia or hyperglycemia.
  • Known allergies or contraindications to ketamine or levetiracetam
  • Failure to obtain intravenous access.

Treatment and study plan

ketamine

Drug

Intravenous ketamine (5 mg/ml concentration) 2 mg/kg (max 90 mg) over 2 minutes

Levetiracetam

Drug

Intravenous levetiracetam (50 mg/ml concentration) 60 mg/kg (max 4500 mg) over 5 minutes

Placebo

Drug

Intravenous isotonic saline 0.4 mL/kg (maximum 18 mL) over 2 minutes

Primary outcomes

  1. Number of participants with cessation of seizures at 20-minute

    Time frame: 20 minutes

    Number of participants with cessation of clinically evident seizures at 20-minute after starting study drug administration without endotracheal intubation or need for other antiseizure medications or anticonvulsant sedatives

Secondary outcomes

  1. Number of participants with cessation of seizures at 5-minute

    Time frame: 5 minutes

    Number of participants with cessation of clinically evident seizures at 5-minute after starting study drug administration

  2. Number of participants with sustained cessation of seizures

    Time frame: From 20 minutes to 60 minutes

    Number of participants with sustained cessation of clinically evident seizures from 20-minute to 60-minute after study drug administration with improved responsiveness (verbal communication, obeying commands, or purposeful reaction to painful stimuli) and no endotracheal intubation or use of any additional antiseizure medications or anticonvulsant sedatives.

  3. Number of participants with recurrence of seizures

    Time frame: From 20 minutes to 4 hours

    Number of participants with recurrence of clinically evident seizures after initial control

  4. Number of participants underwent endotracheal intubation

    Time frame: 60 minutes

    Number of participants underwent endotracheal intubation at 60 minutes after starting study drug administration

  5. Number of participants with severe hypotension

    Time frame: 60 minutes

    Number of participants with severe hypotension at 60 minutes after starting study drug administration

  6. Number of participants with severe hypertension

    Time frame: 60 minutes

    Number of participants with severe hypertension at 60 minutes after starting study drug administration

  7. Number of participants with severe cardiac arrhythmia

    Time frame: 60 minutes

    Number of participants with severe cardiac arrhythmia at 60 minutes after starting study drug administration

  8. Number of participants with emergence reactions

    Time frame: 4 hours

    Emergence reactions (hallucination, delirium, vivid dreams, blurred/double vision, hypersalivation) requiring benzodiazepines or other therapies within 4 hours after starting study drug administration

  9. Number of participants admitted to Pediatric Intensive Care Unit

    Time frame: 24 hours

    Number of participants with admitted to Pediatric intensive Care Unit at 24 hours after starting study drug administration

  10. Mortality

    Time frame: 24 hours

    All-cause mortality at 24 hours after starting study drug administration

Study contacts

Contact information is provided by the study sponsor or research team.

Elsayed Abdelkreem, MD, PhD

CONTACT

[email protected]

1114232126 ext. +20

Sponsors and collaborators

Lead sponsor

Sohag University

Other

Registry information

Official study title

Efficacy of Combined Ketamine and Levetiracetam as a Second-line Anti-seizure Medication for Generalized Convulsive Status Epilepticus in Children

Acronym: KLaSSEC

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 1, 2025
Registry last updated
Jul 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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