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Study identifier: NCT07098728 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Levetiracetam Versus Phenobarbital in Benzodiazepines Unresponsive Paediatric Prolonged Seizures

Condition: Seizure  ·  Sponsor: Ministry of Health and Sports, Myanmar

PhaseNA
Planned participants180
Who can joinAll sexes, 1 Month to 12 Years
Healthy volunteersNo

About this study

Convulsive prolonged seizures in children are the most common life-threatening neurological emergencies. The aim of active management of seizure control is to prevent irreversible neuronal damage as early as possible. Although there is evidence of the use of benzodiazepines as the initial management for prolonged seizures, up to a third of patients do not respond to benzodiazepines. Many trials study the rate of seizures control among various second-line antiseizure medications (ASMs) in benzodiazepines unresponsive convulsive prolonged seizures. However, there is still few recommendations for paediatric population which drug is the most effective to control seizures rapidly and there is also a limited data on which drug has less adverse effects and is well tolerated. Currently, injection phenobarbital or levetiracetam is used as second-line antiseizure medication based on expert opinion in many centres globally including Yangon Children's Hospital. From this study, it is expected to identify the safer and more effective second-line treatment for prolonged seizures in children and be helpful in considering the alternative choice of appropriate medications in the management of prolonged seizures to include in the local guideline. A hospital-based randomized comparative study will be conducted at Yangon Children's Hospital. All children with benzodiazepines unresponsive prolonged seizures will be eligible for this study with the minimum sample size of 180 (90:90). Consecutive s…

This description comes directly from the study's public registry record.

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Locations (2)

Yangon Children's HospitalYangon, Yangon, BurmaRecruiting
Yangon Children's HospitalYangon, Yangon, BurmaRecruiting

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Source record: clinicaltrials.gov/study/NCT07098728