About this trial
Postoperative agitation and emergence delirium describe a spectrum of symptoms of early postoperative negative behavior, in which the child experiences a variety of behavioral disturbances including crying, thrashing, and disorientation during early awakening from anaesthesia. The symptoms are common with a reported incidence of approximately 25%. Some clinical trials have studied the effect of prophylactic oral melatonin for reducing the risk of emergence agitation in children, some finding a considerable dose-response effect. Melatonin has a low bio-availability of approximately 15 %. The safety of exogenous melatonin for pediatric patients has been studied with no apparent serious adverse effects, even at repeated short-term use of high doses of intravenous melatonin. The aim of this clinical trial is to investigate the prophylactic effects and safety of intravenous melatonin administered intraoperatively for prevention of postopreative agitation and emergence delirium in children after an elective surgical procedure. The study is designed as a randomised, double-blind, placebo-controlled clinical trial.
Eligibility criteria
Qualifiers
Patients aged 1-6 years
Elective surgical procedure of en axpected duration of at least 30 minutes in general anesthesia maintained with sevoflurane
Disqualifiers
Any known allergy or contraindication to study treatment or excipåients
Current daily medication with melatonin
Trial design
Treatments tested in this trial
- Melatonin
- Isotonic sodium chloride solution
Treatment groups
Sponsors and collaborators
Rigshospitalet, Denmark
Lead sponsor
Sygehus Lillebaelt
Collaborator
University of Copenhagen
Collaborator
Copenhagen Trial Unit, Center for Clinical Intervention Research
Collaborator