About this trial
For pediatric patients undergoing general anesthesia, poor anesthesia induction compliance often has adverse effects on individual behavior in the early postoperative period. Dexmedetomidine can reduce the cardiovascular responses and postoperative mental adverse reactions caused by esketamine anesthesia induction \[6\]. This study aims to explore the ED50 and ED95 and clinical effects of the combination of dexmedetomidine and esketamine nasal drops for preoperative sedation in children of different ages undergoing general anesthesia, providing a theoretical basis for the combined use of dexmedetomidine and esketamine for preoperative sedation in children undergoing general anesthesia.
Eligibility criteria
Qualifiers
ASA physical status classification Grade I or II;
Age 1-6 years old;
Children who need to undergo general anesthesia for elective surgery;
Weight within the normal range;
Disqualifiers
The child's guardian or the child themselves refuses to participate in the study;
Patients with contraindications for sedation/anesthesia or a history of abnormal recovery from sedation/anesthesia;
Individuals known to be allergic to the study drugs, opioid drugs, or rescue medications;
Individuals with a history of heart, brain, liver, kidney, or metabolic diseases;
Trial design
Treatments tested in this trial
- dexmedetomidine
- Esketamine