Actively Recruiting
High-Flow Nasal Oxygen for Preoxygenation in Emergency Surgery Patients With Full Stomachs
Led by Nguyen Dang Thu · Updated on 2025-03-17
200
Participants Needed
1
Research Sites
180 weeks
Total Duration
On this page
Sponsors
N
Nguyen Dang Thu
Lead Sponsor
H
Hanoi Medical University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Patients with full stomachs face a high risk of regurgitation and aspiration under general anesthesia. To minimize the time between the loss of airway protective reflexes and successful tracheal intubation, rapid sequence induction intubation is commonly used. However, these patients are particularly vulnerable to hypoxemia during anesthesia induction, especially in emergency cases. Pre-oxygenation before induction is crucial for ensuring patient safety during apnea. High-flow nasal oxygen (HFNO) therapy, which consists of an air/oxygen blender, an active humidifier, and a single heated circuit, has recently gained widespread use in intensive care units (ICUs) for managing hypoxemic respiratory failure. HFNC can deliver a constant fraction of inspired oxygen (FiO₂) from 0.21 to 1.0 at high flow rates (up to 60 L/min or higher). Its advantages include generating continuous positive airway pressure, reducing anatomical dead space, improving ventilation-perfusion matching, enhancing mucociliary clearance, and decreasing the work of breathing. Given these benefits, HFNO has the potential to improve pre-oxygenation before and during anesthesia induction in emergency surgery patients with full stomachs.
CONDITIONS
Official Title
High-Flow Nasal Oxygen for Preoxygenation in Emergency Surgery Patients With Full Stomachs
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Emergency surgical patients at risk of gastric fullness requiring endotracheal intubation
- Patients aged 18 years or older
- Health status classified as ASA I or II
- Mallampati classification I or II
You will not qualify if you...
- Patients with a predicted difficult airway, facial deformities, or an inability to achieve a proper mask seal
- Patients with respiratory diseases
- Pregnant patients
- Patients allergic to anesthesia or resuscitation drugs
- Patients who do not consent to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Anesthesia, Phu Tho General Hospital
Viet Tri, Phu Tho, Vietnam, 290000
Actively Recruiting
Research Team
H
Hong Bui Minh, M.D
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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