Skip to main content
Clinical Trials/NCT03709524
NCT03709524
Completed
Not Applicable

A Comparison of Airtraq and Nasotracheal Airtraq for Orotracheal Intubation

Kocaeli University1 site in 1 country119 target enrollmentOctober 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Difficult Intubation
Sponsor
Kocaeli University
Enrollment
119
Locations
1
Primary Endpoint
Intubation time
Status
Completed
Last Updated
6 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 15, 2018
End Date
February 20, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Zehra Ipek ARSLAN

Associate Professor

Kocaeli University

Eligibility Criteria

Inclusion Criteria

  • \> 18 AGE
  • requiring endotracheal intubation

Exclusion Criteria

  • \< 18 AGE
  • ASA III-IV
  • upper respiratory infection past ten days

Outcomes

Primary Outcomes

Intubation time

Time Frame: 6 months

entering the oral cavity till intubation

Secondary Outcomes

  • insertion time(6 months)

Study Sites (1)

Loading locations...

Similar Trials