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Oral Melatonin Versus Nebulized Dexmedetomidine on Emergence Agitation in Children Undergoing Adenotonsillectomy

RecruitingNAAges 3 Years - 7 YearsAllTanta University
NCT07345715 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study aims to compare the efficacy of using oral Melatonin versus nebulized Dexmedetomidine in limitation of emergence agitation in children undergoing adenotonsillectomy.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Children aged between 3 and 7 years. * Both sexes. * Classified as American Society of Anesthesiologists (ASA) physical status I or II according to the American Society of Anesthesiologists. * Scheduled for elective adenotonsillectomy under general anesthesia. Exclusion Criteria: * Parental refusal to participate in the study. * Known allergy or hypersensitivity to dexmedetomidine, melatonin or midazolam. * Presence of developmental delay. * Central nervous system disorders. * Intellectual disability (formerly termed mental retardation). * Neurological or psychiatric conditions associated with anxiety or agitation (e.g., cerebral palsy, epilepsy, separation anxiety disorder, attention-deficit/hyperactivity disorder). * Current or recent treatment with anticonvulsants or sedative medications
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What it tests

  • Normal saline
  • Oral melatonin syrup
  • Nebulized dexmedetomidine
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Where

1 site
Tanta University
Tanta, Egypt
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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