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Clinical Trials in China / NCT06425406
Recruiting Not applicable

Application of HFNC for the Prevention of Hypoxemia During Perioperative Anesthetic-induced Intubation in Children: A Randomized Controlled Clinical Trial

NCT06425406 · tracked via the Priya Life Science China tracker
Sponsor
Henan Provincial People's Hospital
Phase
Not applicable
Started
2024-06-15
Last updated
2025-12-01

Condition(s) studied

High-flow Nasal CannulaChildrenPre-oxygenation

Investigational drug(s) / intervention(s)

high-flow nasal cannula

high-flow nasal cannula: In group H, mask ventilation was performed after the patient lost spontaneous breathing until the end-expiratory oxygen concentration reached 90 %. The lower mask was taken and HFNC was used to record the patient 's safe apnea time.

Study summary

Compared with adults, children have higher metabolic needs, and the airway is more likely to collapse. Before tracheal intubation after anesthesia induction, the patient 's spontaneous breathing completely disappears. At this critical stage, the residual oxygen of the lung is consumed, resulting in hypoxemia and atelectasis. Therefore, it is necessary to explore the best oxygenation strategy during intubation. In addition, ultrasound has become a common equipment in the operating room. It has the advantages of portability, repeatability, and no radiation, and can provide strong support for the diagnosis of gastric distension.

Eligibility

Sex
ALL
Min age
2 Years
Max age
10 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age 2-10 years old; * American Society of Anesthesiologists (ASA) Level I or II; * Children with healthy lungs and hearts; * Clear headed and able to cooperate with anesthesiologists for treatment. Exclusion Criteria: * Contraindications for HFNC: (1) Complete obstruction of the upper respiratory tract; (2) Skull base fracture or nasal bone fracture; (3) Patients who refuse to use HFNC; * The American Society of Anesthesiologists (ASA) rating is greater than Level II; * Children with upper respiratory tract infections within 2 weeks; * Pulmonary dysfunction, congenital heart disease in children;

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Anaesthesiology and Perioperative Medicine, People's Hospital of Zhengzhou University, Henan Provincial People's Hospital Zhengzhou Henan Recruiting

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Other trials for the same condition

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 NCT06425406 on ClinicalTrials.gov ↗ ← All trials in China