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Conox-Guided Anesthesia in Pediatric Adenotonsillectomy
Sponsor: Kayseri City Hospital
Summary
This study aims to evaluate the effect of Conox (qCON/qNOX)-guided anesthesia on intraoperative anesthetic drug consumption and postoperative outcomes in pediatric patients undergoing adenotonsillectomy. Conox is a non-invasive EEG-based monitoring system that provides indices of both hypnosis and nociception. In this randomized controlled trial, children aged 3-12 years will be assigned to either a Conox-guided anesthesia group or a standard monitoring group. The primary outcome of the study is total intraoperative opioid consumption, assessed from anesthesia induction to the end of surgery. Secondary outcomes include emergence time, extubation time, postoperative agitation, pain scores, and correlation between qCON/qNOX values and hemodynamic parameters.
Official title: A Randomized Controlled Trial Evaluating the Effect of qCON/qNOX-Guided Anesthesia on Clinical Outcomes in Pediatric Adenotonsillectomy
Key Details
Gender
All
Age Range
3 Years - 12 Years
Study Type
INTERVENTIONAL
Enrollment
128
Start Date
2026-03-01
Completion Date
2026-09-01
Last Updated
2026-05-11
Healthy Volunteers
No
Interventions
Conox Monitor
EEG-based monitoring device providing qCON and qNOX indices to guide anesthetic depth and analgesia.
Standard Anesthesia Monitoring
Anesthesia management based on conventional clinical parameters such as heart rate and blood pressure.
Locations (1)
Kayseri Şehir Hastanesi
Kayseri, Turkey (Türkiye)