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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04291339
Other study ID # 4-2019-1336
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 11, 2020
Est. completion date January 12, 2021

Study information

Verified date May 2021
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 198
Est. completion date January 12, 2021
Est. primary completion date January 12, 2021
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms

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

Intervention

Procedure:
High-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.
Mask 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.

Locations

Country Name City State
Korea, Republic of Severance Hospital, Yonsei University Health System Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak oxygen reserve index value Oxygen reserve index will be monitored continuously during anesthetic induction. for 10 minutes during anesthetic induction. At Day 0.
Secondary The time to achieve the peak oxygen reserve index value Oxygen reserve index will be monitored continuously during anesthetic induction. for 10 minutes during anesthetic induction. At Day 0.
See also
  Status Clinical Trial Phase
Not yet recruiting NCT05571982 - Comparison of the Efficacy of Tidal Volume Breathing and Vital Capacity Breathing During High-flow Nasal Oxygen N/A