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

Airtraq in Obese and Nonobese Men

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05927519
Enrollment
80
Registered
2023-07-03
Start date
2024-10-25
Completion date
2027-10-05
Last updated
2024-10-28

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

Conditions

Intubation; Difficult or Failed, Men, Obesity, Morbid, Video Laryngoscope

Brief summary

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.

Detailed description

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, need of optimization menuvers, perioperative hemodynamic variables, and postoperative complications will also be recorded.

Interventions

DEVICEairtraq video laryngoscope

airtraq video laryngoscope will be used for intubations

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

the participant and the outcome assessor will not know which device was used in this trail

Intervention model description

Airtraq video laryngoscope will be used in morbid obese and non obese patients

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

\> 18 age men gender elective operation requring intuabtion -

Exclusion criteria

\<18 age women emergency operation \-

Design outcomes

Primary

MeasureTime frameDescription
intubation time50 secondsthe intubation time will be recorded beginning the insertion of the Airtraq through the mouth still the endotracheal tube seen passing through the vocal cords

Secondary

MeasureTime frameDescription
insertion time20 secondsinserting the Airtraq through the mouth till the optimal glottic vizualization occurred
peroperative hemodynamic variable4 hoursheart rate

Countries

Turkey (Türkiye)

Contacts

Primary ContactZehra Arslan, professor
zehraipek48@gmail.com00902623038168

Outcome results

None listed

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