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Clinical Trials in China / NCT07108218
Starting soon Not applicable

Lateral Positioning for Extubation After Adenotonsillectomy

NCT07108218 · tracked via the Priya Life Science China tracker
Sponsor
Sichuan University
Phase
Not applicable
Started
2025-08-20
Last updated
2025-08-06

Condition(s) studied

Perioperative Respiratory Adverse EventsAdenoidectomyTonsillectomyChildren

Investigational drug(s) / intervention(s)

lateral postionsupine position

lateral postion: The children will be positioned on their sides with their heads elevated by 30°, a thin pillow behind their backs, the upper legs bent, and the lower legs straightened.

supine position: The children will be changed to a supine flat-lying position for extubation.

Study summary

The postoperative recovery period following general anesthesia has been associated with a 30%-50% incidence of postoperative respiratory adverse events (PRAEs) in pediatric populations, including laryngospasm, airway obstruction, and hypoxemia. Despite the limited effects of existing pharmacological and operative interventions, positional optimization (e.g., lateral or semirecumbent position) may play a potential role by decreasing airway resistance and improving oxygenation. However, evidence-based evidence for its use in pediatric populations is still lacking, necessitating the urgent need for randomized controlled trials.

Eligibility

Sex
ALL
Min age
1 Year
Max age
6 Years
Healthy volunteers
No
Inclusion criteria: 1. Subjects aged 1-6 years old without gender limit. 2. Scheduled for an ambulatory adenotonsillectomy under general anesthesia. 3. American Society of Anesthesiologists (ASA) classification grade I or II. 4. Informed consent obtained from the patients' parents or legal guardians, who have expressed willingness to cooperate. Exclusion criteria: 1. Presence of concomitant cardiac or pulmonary dysfunction or other significant systemic comorbidities. 2. History of difficult airway management or congenital/acquired structural anomalies of the airway. 3. Active respiratory tract infection within 30 days preceding surgery. 4. Preoperative neurological disorders or developmental abnormalities. 5. Intraoperative occurrence of major complications necessitating deviation from the planned anesthesia protocol or surgical procedure.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
West China Hospital Chengdu Sichuan

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07108218 on ClinicalTrials.gov ↗ ← All trials in China