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CompletedNCT05559502Updated Sep 4, 2026

High Flow Nasal Oxygenation vs Endotracheal Intubation on Recovery Profiles in Laryngeal Microsurgery

An interventional study of HFNO group and ET group in Cough, sponsored by Ajou University School of Medicine. Completed at 1 site in South Korea. Open to participants aged 19 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-04.

Sponsored by Ajou University School of Medicine · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
19 Years to 80 Years
Sex
All
01

Study summary

Transnasal humidified rapid-insufflation ventilatory exchange(THRIVE), or also termed high flow nasal oxygenation (HFNO) is a method of supplying heated, humidified high concentrations of oxygen via nasal cavity. This study hypothesizes that in general anesthesia for laryngeal microsurgery, high-flow nasal oxygen without endotracheal intubation reduces cough during the emergence period compared to endotracheal intubation.

Read the detailed description

Laryngeal microsurgery is mainly performed by a conventional method of general anesthesia with endotracheal intubation (ET), which may have difficulty accessing the lesion behind the larynx, and may be limited in securing space for surgical manipulation. To compensate for these shortcomings, a method of maintaining general anesthesia without using an endotracheal tube has been introduced, and high-flow nasal oxygen(HFNO) and transnasal humidified rapid insufflation ventilatory exchange(THRIVE) enable tubeless anesthesia due to apnea oxygenation and apnea ventilation effect during laryngeal microsurgery. Coughing and straining can be accompanied by emergence after general anesthesia. Forceful vocal cord adduction especially after upper respiratory surgery such as laryngeal microsurgery can cause damage and bleeding of surgical tissue, delaying wound healing. If a small amount of remifentanil is continuously injected during emergence after total intravenous anesthesia(TIVA), airway complications such as coughing can be reduced during emergence without delay in recovery time, and hemodynamic stability can be promoted. In this study, the effect of endotracheal intubation and high-flow nasal oxygen on the emergence cough and postoperative sore throat is compared when total intravenous anesthesia(TIVA) using propofol and remifentanil is performed in patients undergoing laryngeal microsurgery. This study hypothesizes that in general anesthesia for laryngeal microsurgery, high-flow nasal oxygen without endotracheal intubation reduces cough during the emergence period compared to endotracheal intubation.

02

Conditions studied

  • Cough

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Keywords

  • High flow nasal oxygenation
  • Laryngeal microsurgery
  • emergence cough
03

In context

Cough

346 studies on the registry are indexed under Cough; 71 are open to participants now.

This study's enrollment of 52 is below the median of 70 across 263 interventional studies indexed under Cough.

Browse Cough studies →

Lead sponsor

Ajou University School of Medicine is the lead sponsor of 171 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with American Society of Anesthesiologists classification 1 or 2 who receive general anesthesia for laryngeal microsurgery

Exclusion criteria

Exclusion Criteria:

  • Patients with major cardiovascular, pulmonary, and cerebrovascular disease
  • Laser laryngeal surgery
  • Morbid obesity (BMI>35 kg/m2)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
52 participants (actual)

Study arms

  • Experimental
    HFNO group

    Patients will receive HFNO therapy during laryngomicrosurgery.

    Device: HFNO group

  • Active comparator
    ET group

    Endotracheal intubation was performed for general anesthesia

    Device: ET group

Interventions

  • DeviceHFNO group

    HFNO therapy make possible to perform tubeless anesthesia, providing perfect exposure of structure of the vocal cords.

    Also known as: Optiflow

  • DeviceET group

    Endotracheal tube is a plain tube, which is most commonly used in general anesthesia.

    Also known as: Portex, Smiths Medical International Ltd., South East England, United Kingdom

06

What researchers measure

Primary outcomes

  1. Grade of Emergence cough during periextubation period

    Grade Score (grade 0=no cough, grade 1=light or single cough, grade 2=moderate cough or more than one episode of nonsustained coughing, grade 3=sustained and repetitive cough movements with head lift, 0 is the minimum value which is a better outcome and 3 is the maximum value which is a worse outcome.)

    Time frame: From end of surgery to extubation

Secondary outcomes

  1. Number of Participants with postoperative airway complications

    post operative sore throat

    Time frame: from 1 hour after surgery to 24 hours after surgery

07

Study locations

1 site
  • Ajou University Hospital
    Suwon, Gyeongki-do 443-721, South Korea
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05559502
Lead sponsor
Ajou University School of Medicine
Responsible party
Jong Yeop Kim (Professor, Ajou University School of Medicine) — Principal investigator
First posted
Sep 29, 2022
Start date
Nov 15, 2022
Primary completion
Jun 16, 2026
Completion
Jun 17, 2026
Last update
Sep 4, 2026

Study contacts

JongYeop Kim, M.D.,Ph.D.
principal investigator · Ajou University School of Medicine

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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