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Recruiting NCT07095842

Prehospital Early Administration of Ketamine for Status Epilepticus in Epileptic Kids (PEAK-SEEK)

Phase II / Phase III Interventional Convulsive Status EPILEPTICUS

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ketamine, Midazolam.
Who it may be relevant to
Registry conditions: Convulsive Status EPILEPTICUS. Basic parameters: 2 years — 16 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Efficacy of Add-on Ketamine With Second-dose Midazolam for Prehospital Treatment of Epileptic Children With Status Epilepticus

Overview

The goal of this pragmatic, decentralized, pre-consented, event-driven, randomized controlled trial is to investigate the efficacy of add-on ketamine to second-dose midazolam for prehospital treatment of epileptic children with convulsive status epilepticus.

Detailed description

Status epilepticus (SE) is the most prevalent neurological emergency in children. Benzodiazepines (BDZs) remain the first-line anti-seizure medication (ASM) for SE, but about one-third of seizures are not controlled by BDZs. Moreover, second-line ASMs (levetiracetam, valproate, phenytoin) fail to terminate BDZ-refractory SE in 50% of cases. Such prolonged SE is linked with progressive brain damage and an increased risk of epilepsy, irreversible neurodevelopmental sequelae, and mortality. Accordingly, early control of SE is critical for enhancing clinical outcomes.

A possible strategy for rapid control of SE is using early ASM combination. Ketamine seems a promising choice for such a combination. Ketamine acts to antagonize N-methyl-D-aspartate (NMDA) receptors, which become increasingly upregulated and trafficked to the synaptic membrane during ongoing seizure activity. Numerous observational studies have demonstrated that administration of ketamine is associated with termination or attenuation of refractory SE (RSE) and super-refractory SE (SRSE). Furthermore, the recently published Ket-Mid study showed that the ketamine-midazolam combination was more effective than midazolam alone in the initial treatment of pediatric generalized CSE. However, the Ket-Mid study also highlighted a significant delay in hospital arrival and administration of first-line ASM, by a median of 34 minutes, reflecting delayed access to emergency care due to socioeconomic challenges, geographic barriers, and limited prehospital emergency medical services. Such a challenge also applies to resource-limited settings, where treatment delays are more common. Notably, a review by Gaínza-Lein et al. of 15 studies involving 2212 patients with SE reported average times to ASM treatment and hospital arrival of 42.4 and 56 minutes, respectively. Such delay to the administration of ASM is associated with increased resistance to BZDs, longer SE, and increased risk of complications. Accordingly, there is a growing interest in the early use of ASM for prehospital treatment of SE.

Ketamine has been used in prehospital setting for a long time, mainly for sedation and analgesia purposes with a high safety profile. Multiple observational studies have reported the efficacy of ketamine in the pre-hospital emergency treatment of BZD-refractory status epilepticus. However, this was not adequately investigated in clinical trials.

The present study (Prehospital Early Administration of Ketamine for Status Epilepticus in Epileptic Kids, PEAK-SEEK) aims to investigate the efficacy of adding ketamine to second-dose midazolam vs. second-dose midazolam alone as ASM for prehospital treatment of epileptic children with convulsive status epilepticus.

Interventions

  • Drug Ketamine
    Intramuscular ketamine 2 mg/kg (max 90 mg)
  • Drug Midazolam
    Intramuscular midazolam 0.2 mg/kg (max 10 mg)

Primary outcome measures

  • Number of participants with cessation of seizures at the time of hospital arrival [Time frame: At the time of hospital arrival (up to 1 hour)]
Secondary outcome measures (7)
  • Number of participants with sustained cessation of seizures [Time frame: From 10 minutes after study drug administration to 60-minutes after hospital arrival]
  • Number of participants with recurrence of seizures [Time frame: From 10 minutes after study drug administration to 60-minutes after hospital arrival]
  • Number of participants underwent endotracheal intubation [Time frame: 60 minutes after hospital arrival]
  • Number of participants with severe hypotension [Time frame: At the time of hospital arrival (up to 1 hour)]
  • Number of participants with severe hypertension [Time frame: At the time of hospital arrival (up to 1 hour)]
  • Number of participants with severe cardiac arrhythmia [Time frame: At the time of hospital arrival (up to 1 hour)]
  • Number of participants with emergence reactions [Time frame: At the time of hospital arrival (up to 1 hour)]

Eligibility criteria

Inclusion criteria

  • Age from 2 to 16 years.
  • Established diagnosis of epilepsy of at least 1 year duration.
  • History of at least 1 episode of convulsive status epilepticus in the preceding 12 months.

Exclusion criteria

  • Failure to obtain informed consent.
  • Known allergies or contraindications to ketamine.
  • Known contraindications to intramuscular injection.
  • Presence of another family member included in the same trial.
  • Having subsequent events (only the index event will be included).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Department of Pediatrics at Sohag University Hospital — Sohag

Identifiers

NCT: NCT07095842 · Soh-Med-25-7-4PD

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗