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RECRUITING Not applicable ClinicalTrials.gov

Impact of Neuromonitoring on Postoperative Agitation in Pediatric General Anesthesia

Sponsor: Sakarya University • ClinicalTrials.gov ID: NCT07243990

Registry updated: 2026-09-09
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Description

Postoperative agitation is frequently observed in the pediatric patient group following general anesthesia. The exact cause of this agitation has not been clearly determined; however, it may be associated with various factors such as anesthesia depth, family approach, postoperative pain, or unpleasant odors perceived by the child. The depth of anesthesia is indirectly monitored by observing the patient's blood pressure, heart rate, and oxygen saturation, as well as by assessing the alveolar concentration of the inhalation agent. Patients under anesthesia are in a state of deep sleep. In recent years, this sleep state has begun to be monitored more closely with the development of new devices. Electroencephalography (EEG) is a test that records and measures the brain's electrical activity, providing information about the depth of sleep according to the patient's brain activity. The Density Spectral Array (DSA) device, developed for use in operating rooms, facilitates the interpretation of EEG data and guides the anesthesiologist. In our operating room, patients under anesthesia are also monitored using this device. Our aim is to evaluate emergence agitation in patients monitored with this device compared to those who are not monitored.

Interventions

  • dsa intervention group (Device)
    The Density Spectral Array (DSA) device, developed for use in operating rooms, facilitates the interpretation of Electroencephalogram (EEG) data and guides the anesthesiologist. In our operating room, patients under anesthesia are also monitored using this device.
  • Traditional Monitoring (Other)
    This group will receive anesthesia induction using the traditional method, and monitoring will continue simultaneously with EEG (Electroencephalography).

Eligibility criteria

Inclusion Criteria: Patients aged 6-12 years Without chronic comorbid conditions No history of epilepsy Presenting for surgery with preserved consciousness, oriented and cooperative Exclusion Criteria: Intracranial surgeries Intellectual disability Emergency trauma cases Forehead area unsuitable for electrode placement

Conditions

Postoperative Agitation Emergence Delirium, Anesthesia

Locations

  • Sakarya University Training and Research Hospital — Sakarya, Turkey (Türkiye)
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record