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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05851664
Other study ID # Time to intubate VL
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date April 30, 2023

Study information

Verified date May 2023
Source Mongi Slim Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The Aim of the study was to determine the impact of the videolaryngoscpe on the time needed to intubate. This was a Prospective, randomized, simple blinded study. The participants intubated patients for surgery under general anesthesia either with direct laryngoscpy or with videolaryngoscopy.


Description:

Intubation on full stomach is at high risk of pulmonary suction. It must be quick, as this risk increases with the time needed to intubate. Videolaryngoscope (VL) is recommended in case of difficult airway. Yet, its interest in full stomach remains unclear, as the time needed to intubate with a VL is variable in literature. The Aim of the study was to determine the impact of the videolaryngoscpe on the time needed to intubate. This was a Prospective, randomized, simple blinded study. The participants intubated patients for surgery under general anesthesia either with direct laryngoscpy or with videolaryngoscopy.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date April 30, 2023
Est. primary completion date March 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age > 18 years-old; - ASA status 1 to 3; - General anesthesia and intubation. Exclusion Criteria: - Difficult intubations criteria.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
intubation by direct laryngoscopy
intubation using a direct laryngoscopy type macintosh
Intubation by videolaryngoscopy
Intubation using a videolaryngoscope type McGrath

Locations

Country Name City State
Tunisia Mongi Slim hospital Tunis

Sponsors (1)

Lead Sponsor Collaborator
Mongi Slim Hospital

Country where clinical trial is conducted

Tunisia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time needed to intubate Time needed to the operator to pass the tube through vocal cords in seconds during the intubation
Secondary Difficulty of the laryngoscopy cormack anf lehane grade (1 to 4) 1 and 2 indicate easy laryngoscopy and 3 and 4 indicate difficult laryngoscopy at the end of intubation
Secondary Number of intubation attempts. number of attempts needed to intubate at the end of intubation
Secondary Major desaturation an oximetry under 90 % during intubation
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