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Comparison of the Efficacy of High-flow Nasal Oxygen Therapy and Facial Mask Ventilation on the Increase of the Oxygen Reserve Index During Anesthetic Induction

Comparison of the Efficacy of High-flow Nasal Oxygen Therapy and Facial Mask Ventilation on the Increase of the Oxygen Reserve Index During Anesthetic Induction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04291339
Enrollment
198
Registered
2020-03-02
Start date
2020-11-11
Completion date
2021-01-12
Last updated
2021-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult Patients 20 Years of Age or Older Who Are Planning to Undergo Surgery Under General Anesthesia

Brief summary

The purpose of this study is to compare the ability of oxygenation with high-flow nasal oxygen therapy and mask ventilation technique for induction of anesthesia in adult patients who are planning to undergo surgery under general anesthesia.

Interventions

PROCEDUREHigh-flow nasal oxygen technique

High-flow nasal oxygen will be applied to the patients through nasal openings using Optiflow system during anesthetic induction. Pulse oximetry and oxygen reserve index will be monitored continuously.

PROCEDUREMask ventilation technique

Oxygen will be supplied through the mouth and nose to the patients using facial mask during anesthetic induction. Pulse oximetry and oxygen reserve index will be monitored continuously.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult patients aged over 19 years who are scheduled for sleep endoscopy

Exclusion criteria

* basal skull fracture * facial anomaly * consciousness disorder * Risk of aspiration * necessity of awake fiberoptic intubation due to the large vocal cord mass, endotracheal tumor or bleeding.

Design outcomes

Primary

MeasureTime frameDescription
Peak oxygen reserve index valuefor 10 minutes during anesthetic induction. At Day 0.Oxygen reserve index will be monitored continuously during anesthetic induction.

Secondary

MeasureTime frameDescription
The time to achieve the peak oxygen reserve index valuefor 10 minutes during anesthetic induction. At Day 0.Oxygen reserve index will be monitored continuously during anesthetic induction.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026