Conox-Guided Anesthesia in Pediatric Adenotonsillectomy
Recruiting
N/A
Interventional Study
Adenotonsillar Hypertrophy
Postoperative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 3 – 12
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 128 (estimated)
- Sponsor
- Kayseri City Hospital · Government
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About This Trial
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 eithe…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Children aged 3 to 12 years ASA physical status I-II Scheduled for elective adenotonsillectomy No acute infection or systemic disease Parent or legal guardian able to provide written informed consent
Exclusion Criteria:
Skin lesions or anatomical abnormalities preventing place…
Contacts
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