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Orotracheal Intubation in Adult Patients: A Comparison of Standard Airtraq , Nasotracheal Airtraq Combined With a Stylet Inserted Endotracheal Tube and Standard Airtraq Combined Fiberoptic Intubation

A Comparison of Airtraq and Nasotracheal Airtraq for Orotracheal Intubation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03709524
Enrollment
119
Registered
2018-10-17
Start date
2018-10-15
Completion date
2019-02-20
Last updated
2019-06-28

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

Conditions

Difficult Intubation

Brief summary

Adult patients requiring endotracheal intubation divided into three groups; standard Airtraq, Nasotracheal Airtraq + styletted endotracheal tube and Airtraq + fiberoptic combination groups.

Detailed description

We enroll lean adult patients requiring endotracheal intubation. Using a sealed envelope technique they divided into three groups; Standard Airtraq and Nasotracheal Airtraq + styletted endotracheal tube and Standard Airtraq + fiberoptic combination. Demographic characteristics and airway management variables such; age, gender, height, weight, ASA status, tooth morphology, tiro mental and sternomental distance were recorded. Insertion times, intubation times and total intubation times with these devices will be recorded. Hemodynamic parameters recorded such as; heart rate will be recorded baseline , after anesthesia, after insertion, just after and then every 2 minutes intervals after intubation. sore throat, hoarseness, dysphasia, bronchospasm were also recorded postoperatively.

Interventions

DEVICEAirtraq + fiberoptic

video laryngoscope with a monitor

DEVICEAirtraq

video laryngoscope with a monitor

DEVICENasotracheal Airtraq + styletted tube

video laryngoscope with a monitor

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* BMI\<30 * \> 18 AGE * requiring endotracheal intubation * ASA 1-2

Exclusion criteria

* BMI\> 30 * \< 18 AGE * ASA III-IV * upper respiratory infection past ten days * pregnant

Design outcomes

Primary

MeasureTime frameDescription
Intubation time6 monthsentering the oral cavity till intubation

Secondary

MeasureTime frameDescription
insertion time6 monthsentering the oral cavity till the optimal visualization

Countries

Turkey (Türkiye)

Outcome results

None listed

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