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

NCT ID: NCT03709524

Last Updated: 2019-06-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

119 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-10-15

Study Completion Date

2019-02-20

Brief Summary

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

Detailed Description

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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.

Conditions

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Difficult Intubation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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insertion time

1 minute Airtraq, nasotracheal Airtraq + styletted tube and airtraq + fiberoptic

Group Type ACTIVE_COMPARATOR

Airtraq + fiberoptic

Intervention Type DEVICE

video laryngoscope with a monitor

Airtraq

Intervention Type DEVICE

video laryngoscope with a monitor

Nasotracheal Airtraq + styletted tube

Intervention Type DEVICE

video laryngoscope with a monitor

intubation time

2 minutesAirtraq, nasotracheal Airtraq + styletted tube and airtraq + fiberoptic

Group Type ACTIVE_COMPARATOR

Airtraq + fiberoptic

Intervention Type DEVICE

video laryngoscope with a monitor

Airtraq

Intervention Type DEVICE

video laryngoscope with a monitor

Nasotracheal Airtraq + styletted tube

Intervention Type DEVICE

video laryngoscope with a monitor

Interventions

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Airtraq + fiberoptic

video laryngoscope with a monitor

Intervention Type DEVICE

Airtraq

video laryngoscope with a monitor

Intervention Type DEVICE

Nasotracheal Airtraq + styletted tube

video laryngoscope with a monitor

Intervention Type DEVICE

Other Intervention Names

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videolaryngoscope videolaryngoscope videolaryngoscope

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kocaeli University

OTHER

Sponsor Role lead

Responsible Party

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Zehra Ipek ARSLAN

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kocaeli University Medical Faculty

Kocaeli, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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KIA 2018/446

Identifier Type: -

Identifier Source: org_study_id