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OpenTrials
Completed

NCT Number: NCT03709524

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

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

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kocaeli University Medical Faculty

Kocaeli, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Airtraq + fiberoptic

Device

video laryngoscope with a monitor

Other names: videolaryngoscope

Airtraq

Device

video laryngoscope with a monitor

Other names: videolaryngoscope

Nasotracheal Airtraq + styletted tube

Device

video laryngoscope with a monitor

Other names: videolaryngoscope

Primary outcomes

  1. Intubation time

    Time frame: 6 months

    entering the oral cavity till intubation

Secondary outcomes

  1. insertion time

    Time frame: 6 months

    entering the oral cavity till the optimal visualization

Sponsors and collaborators

Lead sponsor

Kocaeli University

Other

Registry information

Official study title

A Comparison of Airtraq and Nasotracheal Airtraq for Orotracheal Intubation

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Oct 17, 2018
Registry last updated
Jun 28, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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