Macintosh Blade Size for Endotracheal Intubation in Operative Rooms

NCT ID: NCT06232837

Last Updated: 2026-02-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

3058 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-22

Study Completion Date

2025-09-20

Brief Summary

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Endotracheal intubation is a frequent procedure in the operating room but optimal Macintosh blade size remains unknown to date.

Detailed Description

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Endotracheal intubation is an extremely frequent procedure in the operating room, in intensive care units and in emergency medicine (in- or out-of-hospital). Apart from special cases of foreseen difficult programmed intubation, direct laryngoscopy remains the most frequently used technique. It requires the use of a handle (short or long), which serves as a light source on which is adapted a Macintosh curved blade, metallic or plastic, single or multiple use. The choice of blade size is based on the experience of the physician. Most often, in adult settings, size 3 or 4 blades are used. The very spartan literature on the subject and the current recommendations do not provide any information on the choice of blade size. Our team (and others) recently concluded that intubation first attempt rates in intensive care units or emergency settings were improved when using shorter Macintosh blade size No3 vs 4 (Godet et al. Intensive Care Medicine 2022 and Landefeld et al. Critical Care Explorations 2023). We therefore wish to evaluate these practices in terms of success of the first laryngoscopy, Cormack-Lehane and POGO (percentage of glottic opening visualized) scores, the need to use an alternative technique or a second operator in operative rooms. The results will be analyzed with regard as a function and experience of the person performing the laryngoscopy, as well as the setting (urgent or scheduled). These data are usually collected during the performance of an endotracheal intubation in a nationwide fashion in French operative rooms.

Conditions

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Intubation Complication Intubation; Difficult or Failed Endotracheal Intubation

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Macintosh blade size 3

Patients intubated using Macintosh blade size 3

Direct laryngoscopy using Macintosh blade

Intervention Type DEVICE

Patients in operative room requiring direct laryngoscopy for endotracheal intubation

Macintosh blade size 4

Patients intubated using Macintosh blade size 4

Direct laryngoscopy using Macintosh blade

Intervention Type DEVICE

Patients in operative room requiring direct laryngoscopy for endotracheal intubation

Interventions

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Direct laryngoscopy using Macintosh blade

Patients in operative room requiring direct laryngoscopy for endotracheal intubation

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Société Française d'Anesthésie-Réanimation (SFAR)

UNKNOWN

Sponsor Role collaborator

University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Thomas Godet, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Clermont-Ferrand University Hospitals

Locations

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CHU Clermont-Ferrand

Clermont-Ferrand, , France

Site Status

Countries

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France

References

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Godet T, De Jong A, Garin C, Guerin R, Rieu B, Borao L, Pereira B, Molinari N, Bazin JE, Jabaudon M, Chanques G, Futier E, Jaber S. Impact of Macintosh blade size on endotracheal intubation success in intensive care units: a retrospective multicenter observational MacSize-ICU study. Intensive Care Med. 2022 Sep;48(9):1176-1184. doi: 10.1007/s00134-022-06832-9. Epub 2022 Aug 16.

Reference Type BACKGROUND
PMID: 35974189 (View on PubMed)

Landefeld KR, Koike S, Ran R, Semler MW, Barnes C, Stempek SB, Janz DR, Rice TW, Russell DW, Self WH, Vonderhaar D, West JR, Casey JD, Khan A. Effect of Laryngoscope Blade Size on First Pass Success of Tracheal Intubation in Critically Ill Adults. Crit Care Explor. 2023 Mar 6;5(3):e0855. doi: 10.1097/CCE.0000000000000855. eCollection 2023 Mar.

Reference Type BACKGROUND
PMID: 36895888 (View on PubMed)

Other Identifiers

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IRB 00010254-2023-081

Identifier Type: -

Identifier Source: org_study_id

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