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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04930419
Other study ID # K170405J
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received
Last updated
Start date June 15, 2021
Est. completion date December 15, 2021

Study information

Verified date May 2021
Source Assistance Publique - Hôpitaux de Paris
Contact Baudoin Clémence
Phone +331 49 95 61 61
Email clemence.baudoin@aphp.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 150
Est. completion date December 15, 2021
Est. primary completion date December 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Device:
Videolaryngoscopy 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
Direct 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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Outcome

Type Measure Description Time frame Safety issue
Primary 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. up to 10 minutes post inclusion
Secondary Number of attempts needed for successful intubation up to 10 minutes post inclusion
Secondary Time to intubate Time 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 up to 10 minutes post inclusion
Secondary Reason of failure of the first-pass success Reasons 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
up to 10 minutes post inclusion
Secondary Proportion of decision of switch in case of failure up to 10 minutes post inclusion
Secondary Proportion of difficult intubations Difficult 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 up to 10 minutes post inclusion
Secondary Glottic view Glottic 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 up to 10 minutes post inclusion
Secondary Proportion of cases who need for tools to optimize up to 10 minutes post inclusion
Secondary Proportion of cases needed crossovers to other rescue techniques up to 10 minutes post inclusion
Secondary Number of complications per and post-intubation up to 10 minutes post inclusion
Secondary Type of complications per and post-intubation up to 10 minutes post inclusion
Secondary Number of deaths up to 10 minutes post inclusion
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