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Clinical Trials/NCT04291339
NCT04291339CompletedNot Applicable

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

Yonsei University1 site in 1 country198 target enrollmentStarted: November 11, 2020Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
198
Locations
1
Primary Endpoint
Peak oxygen reserve index value
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Care Provider)

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts 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.

Outcomes

Primary Outcomes

Peak oxygen reserve index value

Time Frame: for 10 minutes during anesthetic induction. At Day 0.

Oxygen reserve index will be monitored continuously during anesthetic induction.

Secondary Outcomes

  • The time to achieve the peak oxygen reserve index value(for 10 minutes during anesthetic induction. At Day 0.)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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