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Can High-Flow oxygen prevent dangerous dips during difficult intubations?
NCT ID NCT03604120
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Researchers compare two ways to deliver oxygen before and during breathing-tube placement in surgery patients who are hard to intubate. One method uses a high-flow nasal cannula, the other uses a standard face mask. The trial measures how often oxygen levels drop below 95% or require rescue ventilation, and tracks complications. It includes 186 adults at risk of difficult intubation.
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 cannula oxygen therapy
- What this could lead to
- If it works, this could give anesthesiologists a safer way to keep oxygen levels stable when placing a breathing tube in patients with a difficult airway.
- What could go wrong
- The trial is small and focuses on a specific group of surgical patients, so the approach may not work for everyone or in every hospital. High-flow oxygen can also cause discomfort or nosebleeds.
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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186 people
The number who actually took part.
- Started
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Sep 2018
- Finished
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Mar 2021
- 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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18 years and older
- 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 18 years of aged and over * And anticipated difficult intubation * And requiring a rapid sequence induction for laryngoscopic intubation * Or requiring a fiberoptic intubation Exclusion Criteria: * BMI \> 35 * Pulse oxymetry \< 90% in ambient air * Haemodynamic instability * Pregnancy * Protected adult * Lack of consent * Patient already enrolled in another randomized study looking forward improving preoxygenation quality.
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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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Nantes University Hospital
Nantes, 44093, France
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