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Macintosh Blade Size During Laryngoscopy for Endotracheal Intubation. A Prospective Observational Study.

Macintosh Blade Size During Laryngoscopy for Endotracheal Intubation. A Prospective Observational Study.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05059067
Acronym
MacSize
Enrollment
1500
Registered
2021-09-28
Start date
2021-06-15
Completion date
2022-01-01
Last updated
2021-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endotracheal Intubation

Keywords

Intubation, Macintosh blade, Laryngoscopie, Operative room, Intensive Care Unit, Emergency department

Brief summary

Endotracheal intubation is a frequent procedure in the operating room, in intensive care units and in emergency medicine (in- or out-of-hospital) but optimal Macintosh blade size remains unknown to date.

Detailed description

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. 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. 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 whatever the circumstances: operating room, intensive care unit and emergency department (in-hospital) and in the SAMU-SMUR (pre-hospiatl medical service) at Clermont-Ferrand University Hospital.

Interventions

DEVICEDirect laryngoscopy for endotracheal intubation

Patients in operative room, intensive care unit and emergency department requiring direct laryngoscopy for endotracheal intubation

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients must be admitted in an operative room, an intensive care unit (ICU) or an emergency department 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 * 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

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with successful first-pass orotracheal intubationAt intubationThe proportion of patients with successful first-pass orotracheal intubation

Secondary

MeasureTime frameDescription
Severe complications related to intubation_severe collapseAt intubationRate of cardiovascular collapse, defined as systolic blood pressure less than 65 mm Hg recorded at least once or less than 90 mm Hg lasting 30 minutes despite 500-1,000 ml of fluid loading (crystalloids solutions) or requiring introduction or increasing doses by more than 30% of vasoactive support
Moderate complications related to intubation_arrythmiaAt intubationRate of severe ventricular or supraventricular arrhythmia requiring intervention
Severe complications related to intubation_cardiac arrestAt intubationRate of cardiac arrest
Severe complications related to intubation_deathAt intubationRate of death during intubation
Moderate complications related to intubation_difficult intubationAt intubationRate of difficult intubation
Moderate complications related to intubation_oesophageal intubationAt intubationRate of oesophageal intubation
Moderate complications related to intubation_agitationAt intubationRate of agitation
Severe complications related to intubation_hypoxemiaAt intubationRate of severe hypoxemia defined by lowest oxygen saturation (SpO2) \< 80 %
Moderate complications related to intubation_dental injuriesAt intubationRate of dental injuries
Cormack LehaneDuring intubationRate of Cormack-Lehane grade of glottic view
Difficulty of intubationDuring intubationRate of operator-assessed difficulty of intubation
Additional airway equipmentDuring intubationRate of need for additional airway equipment (video laryngoscope, bougie, stylet, fibroscope, cricothyrotomy)
Additional second operatorDuring intubationRate of need for a second operator
POGO (percentage of glottic opening)During intubationRate of POGO grade of glottic view
Moderate complications related to intubation_aspirationAt intubationRate of pulmonary aspiration

Countries

France

Contacts

Primary ContactLise Laclautre
promo_interne_drci@chu-clermontferrand.fr+33 4 73 754963

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026