Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06879600

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Department of Anesthesia, Phu Tho General Hospital

Viet Tri, Phu Tho, Vietnam, 290000

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here