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 type | Interventional |
|---|---|
| Ages | 6 Years to 12 Years |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Sakarya University Academic / other |
| Locations | 1 site (Sakarya) |
| Status | Recruiting |
| Started | September 4, 2026 |
| Main results expected | October 20, 2026 |
| Study ends | November 1, 2026 |
| Registry record updated | November 10, 2026 |
| Trial ID | NCT07243990 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
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Sakarya University Training and Research Hospital
Sakarya, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: esin topkara oğur, MD,ANESTHESIOLOGY RESIDENT
- Email: topkaraesin@gmail.com
- Phone: +905308583166
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.