Which blade size works best for intubation? large study seeks answers
NCT ID NCT06232837
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study looked at over 3,000 adults having surgery to see which size of Macintosh blade (a tool used to guide a breathing tube into the windpipe) works best. The goal was to find out if blade size affects how often the tube goes in on the first try and how often serious problems like low oxygen or low blood pressure occur. The results could help doctors choose the right blade size for safer intubation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors choose the best blade size for safer, faster intubation in routine surgeries.
- What could go wrong
- This is an observational study, not a controlled trial, so it can show patterns but not prove cause and effect. Results may not apply to all patients or settings.
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.
- Participants
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3,058 people
The number who actually took part.
- Started
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Jan 2024
- Finished
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Sep 2025
- 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.
Who is studied
Any patient requiring orotracheal intubation with direct laryngoscopy in first place
- 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 must be admitted in a participating operative room and require mechanical ventilation through an orotracheal tube. * Adult (age ≥ 18 years) * Subjects must be covered by public health insurance * Written informed consent from the patient or proxy (if present) before inclusion or once possible when patient has been included in a context of emergency. Exclusion Criteria: * Anticipated difficult intubation requiring videolaryngoscopy or other technic in first place * Nasotracheal intubation * Refusal of study participation or to pursue the study by the patient * Absence of coverage by the French statutory healthcare insurance system * Protected person
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Genom att skicka in godkänner du våra Användarvillkor
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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CHU Clermont-Ferrand
Clermont-Ferrand, 63000, France
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Other studies related to the condition(s) this trial covers.
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