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Comparative Evaluation of the McGrath Videolaryngoscope and the Direct Laryngoscopy for Tracheal Intubation in the Prehospital Setting

Comparative Evaluation of the McGrath Videolaryngoscope and the Direct Laryngoscopy for Tracheal Intubation in the Prehospital Setting

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04930419
Acronym
AMAC
Enrollment
150
Registered
2021-06-18
Start date
2021-06-15
Completion date
2021-12-15
Last updated
2021-06-18

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

Conditions

Cardio Respiratory Arrest, Indication of Orotracheal Intubation, Neurological Failure, Respiratory Failure

Brief summary

In the prehospital setting, the risk of difficult intubation and life-threatening complications is increased under particular conditions due to the environment or the frequent instability of patients. To limit this risk procedures and devices to ease and secure tracheal intubation must be developped and integrated. As the prevalence of complications increase with the number of attempts of intubation, one strategy is to facilitate the intubation technic itself. Direct laryngoscopy with Macintosh blades is the standard device commonly used in first place for tracheal intubation. Other devices are available and used, mostly for difficult intubation, included videolaryngoscopy. This device has been used and studied for years now. Allowing a better view and glottic visualisation, videolaryngoscopy could increase the first-pass success rate. Among all videolaryngoscopes, the McGrath videolaryngoscope is the most similar device to the standard Macintosh laryngoscope. It is light, compact, with a screen directly linked to the handle, easy to use and offering excellent view. Its usability and efficacy make it a device of choice for the prehospital setting and worth further clinical trials to define its place in the airway strategy. Hypothesis: In the prehospital setting, the use of McGrath videolaryngoscope as the primary device for tracheal intubation could facilitate tracheal intubation and decrease the number of attempts of intubation and complications. The objective of our study is to determine if the use of McGrath videolaryngoscope increase the rate of successful first-pass intubation in the prehospital setting compared to direct view Macintosh laryngoscopy. The primary outcome is the rate of successful intubation at the first attempt. One attempt is defined as an advancement of the tube towards the glottis during a laryngoscopy ; every new try even during the same laryngoscopy is considered as a new attempt. Successful intubation is confirmed by the visualisation of 6 waves of EtCO2.

Interventions

DEVICEVideolaryngoscopy group

Tracheal intubation will be performed using Videolaryngoscope in first intention and will be performed using standard pre-hospital intubation procedures : preoxygenation before intubation, maintenance of oxygenation throughout procedure, standard sedation technique (using rapid sequence intubation (RSI)), correct position confirmation using a capnogram and conditioning (hemodynamic monitoring, respirator settings, securing). If the first attempt at intubation is unsuccessful, further management will be left to the discretion of the clinician according to the procedures and algorithm of usual standard care

DEVICEDirect laryngoscopy group

Tracheal intubation will be performed using Direct laryngoscopy with Macintosh blades in first intention. and will be performed using standard pre-hospital intubation procedures : preoxygenation before intubation, maintenance of oxygenation throughout procedure, standard sedation technique (using rapid sequence intubation (RSI)), correct position confirmation using a capnogram and conditioning (hemodynamic monitoring, respirator settings, securing). If the first attempt at intubation is unsuccessful, further management will be left to the discretion of the clinician according to the procedures and algorithm of usual standard care

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Age more than 18 * Indication of orotracheal intubation * Operators trained to the use of the McGrath

Exclusion criteria

* Pregnancy * No insurance * Major patient under guardianship or curatorship

Design outcomes

Primary

MeasureTime frameDescription
Rate of successful intubation at the first attemptup to 10 minutes post inclusionOne attempt is defined as an advancement of the tube towards the glottis during a laryngoscopy ; every new try even during the same laryngoscopy is considered as a new attempt.Successful intubation is confirmed by the visualisation of 6 waves of EtCO2.

Secondary

MeasureTime frameDescription
Time to intubateup to 10 minutes post inclusionTime to intubate will be defined by the time between the insertion of the device in the mouth and the visualisation of the first waves of EtCO2
Reason of failure of the first-pass successup to 10 minutes post inclusionReasons of failure will be defined as following : * Bad glottic visualization * Difficult progression of the tube towards the glottis despite a good visualisation * Presence of secretions * Presence of foreign body * Presence of fogging on the McGrath * Device failure * Other
Proportion of decision of switch in case of failureup to 10 minutes post inclusion
Proportion of difficult intubationsup to 10 minutes post inclusionDifficult intubation will be evaluated by the intubation difficulty score (score IDS or difficulty of intubation under laryngoscopy score ). It goes from 0 to infinity. zero indicating an easy intubation and infinity being an impossible intubation
Glottic viewup to 10 minutes post inclusionGlottic view will be evaluated with Cormack and Lehane grade and POGO score. POGO score goes from 0 (Visualization of the language base) to 100% (total visualization of the glottis). Cormack and Lehane grade goes from I to IV. A higher Cormack and Lehane grade is worth : I indicate total visualization of the glottis and IV indicate Visualization of the language base
Number of attempts needed for successful intubationup to 10 minutes post inclusion
Proportion of cases needed crossovers to other rescue techniquesup to 10 minutes post inclusion
Number of complications per and post-intubationup to 10 minutes post inclusion
Type of complications per and post-intubationup to 10 minutes post inclusion
Number of deathsup to 10 minutes post inclusion
Proportion of cases who need for tools to optimizeup to 10 minutes post inclusion

Contacts

Primary ContactBaudoin Clémence
clemence.baudoin@aphp.fr+331 49 95 61 61
Backup ContactMatthieu Resche-Rigon
matthieu.resche-rigon@u-paris.fr+33142499773

Outcome results

None listed

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