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Impact of High-flow Nasal Oxygen During Awake Fiberoptic Bronchoscope Guided Intubation: A Retrospective Study

Sponsor
Yonsei University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05022056
Collaborator
(none)
200
Enrollment
1
Location
30
Anticipated Duration (Days)
202.9
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Retrospective data collection. The aim of this study is to investigate impact of high-flow nasal oxygen on safety(lowest oxygen saturation), efficiency (intubation time, need for multiple attempts) in patients underwent awake fiberoptic bronchoscope guided intubation.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    200 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Impact of High-flow Nasal Oxygen During Awake Fiberoptic Bronchoscope Guided Intubation: A Retrospective Study
    Anticipated Study Start Date :
    Sep 1, 2021
    Anticipated Primary Completion Date :
    Oct 1, 2021
    Anticipated Study Completion Date :
    Oct 1, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Intra-procedural lowest saturation [Intra-procedural lowest saturation]

      Intra-procedural lowest saturation: lowest oxygen saturation on pulse oximetry during awake intubation

    2. need for multiple attempts [Intra-procedural (need for multiple attempts : during awake intubation)]

      need for multiple attempts : more than 2 attempts needed during awake intubation

    3. time taken for awake intubation [Intra-procedural (Time taken for awake intubation: time from entering the operating room to completion of awake endotracheal intubation)]

      Time taken for awake intubation: time from entering the operating room to completion of awake endotracheal intubation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    1.Patients who underwent awake fiberoptic bronchoscope guided intubation for surgery

    Exclusion Criteria:

    1. Cases in which other procedures (e.g. arterial line cannulation) were performed prior to endotracheal intubation after entering operation room

    2. Patients with Incomplete records of oxygen saturation, attempt number, and time taken for awake intubation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine Seoul Korea, Republic of

    Sponsors and Collaborators

    • Yonsei University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Yonsei University
    ClinicalTrials.gov Identifier:
    NCT05022056
    Other Study ID Numbers:
    • 4-2021-0901
    First Posted:
    Aug 26, 2021
    Last Update Posted:
    Aug 26, 2021
    Last Verified:
    Aug 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Aug 26, 2021