Could skipping the breathing tube ease recovery after throat surgery?
NCT ID NCT05559502
First seen Sep 04, 2026 ยท Last updated Sep 04, 2026
Summary
This trial tests whether using high-flow nasal oxygen during throat surgery, instead of a breathing tube, can reduce coughing as patients wake up from anesthesia. Researchers will compare 52 adults having laryngeal microsurgery, measuring cough severity and other airway issues like sore throat. The goal is to see if this tubeless approach leads to a smoother, more comfortable recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- High-flow nasal oxygenation (HFNO) using a device called Optiflow, compared with endotracheal intubation using a standard breathing tube.
- What this could lead to
- If it works, this approach could make recovery from throat surgery smoother and more comfortable by reducing coughing and sore throat after anesthesia.
- What could go wrong
- This is a small, early-stage trial, so results may not apply to all patients. HFNO may not suit everyone, and there are risks like airway complications or oxygen levels dropping.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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52 people
The number who actually took part.
- Started
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Nov 2022
- Finished
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Jun 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with American Society of Anesthesiologists classification 1 or 2 who receive general anesthesia for laryngeal microsurgery Exclusion Criteria: * Patients with major cardiovascular, pulmonary, and cerebrovascular disease * Laser laryngeal surgery * Morbid obesity (BMI\>35 kg/m2)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ajou University Hospital
Suwon, Gyeongki-do, 443-721, South Korea
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Other studies related to the condition(s) this trial covers.
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