Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-30
SponsorTunis University
About this trial
The children were randomized into two groups to receive orotracheal intubation after anesthetic induction with neuromuscular blockade, either by direct laryngoscopy (DL, DL group) or by C-MAC video laryngoscopy (VL group)
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
newborns requiring orotracheal intubation for surgery or mechanical ventilation in the intensive care unit
Disqualifiers
age> 01 month
Trial design
Design model
Parallel
Treatments tested in this trial
Video Laryngoscopy
Deviceorotracheal intubation by C-Mac ( Video laryngoscopy)
Direct Laryngoscopy
DeviceOrotracheal intubation using Direct Laryngoscopy
Treatment groups
115 Participants
are divided into 2 treatment groupsGroup A: Video laryngoscopyOther 1 intervention
Group B: Direct laryngoscopyOther 1 intervention
Trial outcomes
Primary outcomes
1
time taken for successful tracheal intubation
Time frame
during intubationSecondary outcomes
1
the need for additional device
Time frame
during intubation2
the number of attempts
Time frame
during intubation3
Complications during intubation
complications such as desaturation and selective intubation.
Time frame
during intubationSponsors and contacts
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Source ClinicalTrials.gov