Comparison of Airtraq in Class 2-3 Obese and Nonobese Men During Intubation: a Prospective Randomized Clinical Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-80
SponsorKocaeli University

About this trial

Morbid obesity is a growing disease. Intubations of these patients mostly difficult. Video laryngoscopes have to be used during the intubation of these patients. The intubation of men is more complicated and difficult than obese women. There were no trials compared to the new video laryngoscopes in morbidly obese men. Patients will be divided into two groups; non-obese and klas 2-3 obese. Airtraq will be used for their intubation. The time for intubation will be the primary aim of this prospective randomized study. The insertion time, perioperative hemodynamic variables, and postoperative complications will also be recorded.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Crossover

Treatments tested in this trial

  • airtraq video laryngoscope

    Device

    airtraq video laryngoscope will be used for intubations

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: morbidly obeseActive comparator 1 intervention
Group B: nonobesePlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

intubation time

the intubation time will be recorded beginning the insertion of the Airtraq through the mouth still the endotracheal tube seen passing through the vocal cords

Time frame
50 seconds

Secondary outcomes

1

insertion time

inserting the Airtraq through the mouth till the optimal glottic vizualization occurred

Time frame
20 seconds
2

peroperative hemodynamic variable

heart rate

Time frame
4 hours

Other outcomes

Sponsors and contacts

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