Clinical trial Recruiting at 1 site Interventional Ages 6 to 12

How monitoring brain activity during anesthesia affects pediatric post-op agitation

Official title: The Effect of Neuromonitoring on the Incidence of Postoperative Agitation in Pediatric Patients Undergoing General Anesthesia

Run by Sakarya University · NCT07243990 · Data updated 2026-11-12

This study tests whether using the Density Spectral Array (DSA) brain-monitoring device during general anesthesia can reduce agitation and delirium after surgery in kids aged 6–12.

Quick facts

Study typeInterventional
Ages6 Years to 12 Years
SexAll
Enrollment80 (estimated)
SponsorSakarya University
Academic / other
Locations1 site (Sakarya)
StatusRecruiting
StartedSeptember 4, 2026
Main results expectedOctober 20, 2026
Study endsNovember 1, 2026
Registry record updatedNovember 10, 2026
Trial IDNCT07243990 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 6–12 without chronic conditions or epilepsy, scheduled for surgery and able to cooperate during preoperative assessment.

Probably not a fit

Children with intracranial conditions, intellectual disability, forehead placement issues, emergency cases, or other disqualifying factors may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial compares standard anesthesia monitoring with an EEG-driven approach using DSA in pediatric patients undergoing surgery. It aims to see if brain activity-guided depth assessment helps lessen emergence agitation and related symptoms after anesthesia. Participants are children aged 6–12 without chronic conditions or epilepsy, undergoing non-emergency procedures. The intervention group uses DSA-based monitoring in addition to traditional measures, while the control group relies on traditional monitoring alone. The study is conducted at Sakarya University Training and Research Hospital under Sakarya University as sponsor.

Why it matters

Potential benefit: If successful, brain-monitoring-guided anesthesia could reduce post-anesthesia agitation and improve recovery in children.

How similar studies have gone: Previous work on EEG-based depth monitoring has shown potential to influence anesthetic management, but evidence in pediatrics for reducing emergence agitation is still evolving.

Who can join: the full rules

Show full inclusion / exclusion 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

Where it's running

  • Sakarya University Training and Research Hospital
    Sakarya, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.