emergence agitation
Conditions
Interventions
group H:Thirty minutes before the end of surgery, group H was administered ciprofol 0.2 mg/kg.
group C:Thirty minutes before the end of the surgery, Group C was administered 0.2 mg/kg of normal saline.
Sponsors
The Third Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
All
Age
3 Years to 8 Years
Inclusion criteria
Inclusion criteria: 1. Age 3-8 years; 2. No gender restriction; 3. Weight 12~30 kg; 4. BMI 18~24 kg/m²; 5. ASA classification I~II; 6. Children scheduled for tonsil low-temperature plasma radiofrequency ablation + adenoid low-temperature plasma surgery under nasal endoscopy.
Exclusion criteria
Exclusion criteria: 1. Recent upper respiratory tract infection; 2. Difficult airway identified during preoperative evaluation; 3. Comorbid dysfunction of vital organs including heart, lungs, brain, liver, and kidneys; 4. Presence of developmental delay; 5. Accompanied by agitation disorder; 6. Existence of cognitive communication impairment; 7. Withdrawal from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative agitation incidence rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Extubation time;heart rate;mean arterial pressure;Number of adverse reactions; | — |
Countries
China
Contacts
Public ContactWei Xiaoyong
The Third Affiliated Hospital of Zhengzhou University
Outcome results
None listed