Conox-Guided Anesthesia in Pediatric Adenotonsillectomy

Recruiting now · Not applicable

Conditions studied: Adenotonsillar Hypertrophy, Postoperative Pain

In brief

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.

Key facts

Study ID
NCT07577154
Run by
Kayseri City Hospital
People needed
128
Starts
2026-03-01
Expected to finish
2026-09-01
Last updated by the study team
2026-05-11

Who can join

Age: 3 and older, up to 12. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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