The goal of this clinical trial is to compare electroencephalogram (EEG) guided propofol sedation versus standard care in paediatric patients aged 6-16 undergoing oesophagogastroduodenoscopy and colonoscopy. The main questions it aims to answer are whether EEG guided propofol sedation will result in: * faster wake up time * reduced time to discharge * reduced cumulative propofol dosage * lower incidence of intraoperative adverse events * no difference in intraoperative undesirable movement * lower incidence and severity of emergence delirium * lower intraoperative depth of sedation Participants will wear an EEG sensor (Sedline) prior to undergoing propofol sedation until they wake up post procedure.
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Time to wake up
Timeframe: Through study completion, approximately 6 months