Overview
The goal of this clinical trial is to compare the Ciprofol and Propofol Under IoC1 and IoC2 Monitoring for Adenotonsillectomy Participants will be randomly allocated to two groups: Ciprofol group (Group C) and Propofol group (Group P). For those in Group C: they will be given ciprofol during anesthesia induction and maintenance .For those in Group P: they will be pgiven ciprofol during anesthesia induction and maintenanc This study evaluates ciprofol versus propofol under IoC1/IoC2 guidance in pediatric T&A, providing evidence for ciprofol's efficacy and safety in pediatric anesthesia.
Eligibility
Inclusion Criteria:
- ASA I/II, age 3-11 years, weight 13-50 kg.
Endoscopic T&A or adenoidectomy.
Exclusion Criteria:
- Recent upper respiratory infection.
Difficult airway, organ dysfunction, developmental/psychiatric disorders.
Drug allergies.