Pediatric Dose Optimization for Seizures in Emergency Medical Services

ConditionSeizures
Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age6-13
SponsorStanford University

About this trial

The Pediatric Dose Optimization for Seizures in Emergency Medical Services (PediDOSE) study is designed to improve how paramedics treat seizures in children on ambulances. Seizures are one of the most common reasons why people call an ambulance for a child, and paramedics typically administer midazolam to stop the seizure. One-third of children with active seizures on ambulances arrive at emergency departments still seizing. Prior research suggests that seizures on ambulances continue due to under-dosing and delayed delivery of medication. Under-dosing happens when calculation errors occur, and delayed medication delivery occurs due to the time required for dose calculation and placement of an intravenous line to give the medication. Seizures stop quickly when standardized medication doses are given as a muscular injection or a nasal spray. This research has primarily been done in adults, and evidence is needed to determine if this is effective and safe in children.

PediDOSE optimizes how paramedics choose the midazolam dose by eliminating calculations and making the dose age-based. This study involves changing the seizure treatment protocols for ambulance services in 20 different cities, in a staggered and randomly-assigned manner.

One aim of PediDOSE is to determine if using age to select one of four standardized doses of midazolam and giving it as a muscular injection or nasal spray is more effective than the current calculation-based method, as measured by the number of children arriving at emergency departments still seizing. The investigators believe that a standardized seizure protocol with age-based doses is more effective than current practice.

Another aim of PediDOSE is to determine if a standardized seizure protocol with age-based doses is just as safe as current practice, since either ongoing seizures or receiving too much midazolam can interfere with breathing. The investigators believe that a standardized seizure protocol with age-based doses is just as safe as current practice, since the seizures may stop faster and these doses are safely used in children in other healthcare settings.

If this study demonstrates that standardized, age-based midazolam dosing is equally safe and more effective in comparison to current practice, the potential impact of this study is a shift in the treatment of pediatric seizures that can be easily implemented in ambulance services across the United States and in other parts of the world.

Eligibility criteria

Qualifiers

Witnessed by the paramedic to be actively seizing, regardless of seizure type or duration; AND

Under the care of a paramedic; AND

Transported by an EMS agency participating in the study

Disqualifiers

A prior history of a benzodiazepine allergy; OR

Known or presumed pregnancy; OR

Severe growth restriction based on the paramedic's subjective assessment

Trial design

Treatments tested in this trial

  • Standardized seizure protocol
  • Conventional seizure protocol

Treatment groups

6,700 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Stanford University

Lead sponsor

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborator

University of Utah

Collaborator

Baylor College of Medicine

Collaborator