Intubation With McGrath Video Laryngoscope and Boedeker Intubation Foreceps in a Population of Patients With Predictors of Difficult Airway

October 24, 2014 updated by: Camilla Strøm, Rigshospitalet, Denmark

Intubation With McGrath Video Laryngoscope and Boedeker Intubation Foreceps in a Population of Patients With Predictors of Difficult Airway, an Observational Pilot Study

Tracheal intubation with videolaryngoscopes have been widely studied, and is now often used in the management of difficult airways.

Videolaryngoscopes with angulated blades can improve laryngeal view, however this does not always match with a higher intubation succes. To adress this matter the aim of this study is gathering experience with intubation with mcgrath videolaryngoscope and a blade-shape intubation foreceps (Boedeker intubation foreceps, Karl Storz, Germany).

The hypothesis is that intubation with this combination is easy and can be a good alternative when using the McGrath videolaryngoscope in patients with predictors of difficult airway.

Study Overview

Study Type

Observational

Enrollment (Actual)

25

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Copenhagen, Denmark, 2100
        • Dept. of Anaesthesia, Centre of Head and Orthopedics 4231, Rigshospitalet

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with one or more predictors of difficult airway

Description

Inclusion Criteria:

  • patients scheduled for elective surgery
  • age over 18 or more
  • planned intubation with mcgrath videolaryngoscope
  • informed conscent obtained
  • patients are
  • patients shall be able to read and understand Danish

Exclusion Criteria:

  • Patients planned to awake intubation
  • stridor
  • hypoxia defined by saturation under 90% without oxygen supply
  • patients with oxygentreatment at home
  • patients that need a wired tube
  • patients that need a preshaped tube
  • patients that need crash induction
  • use of gastric tube

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
airway
Patients with one or more predictors of diffucult airway
Patients will be intubated with the Mcgrath videolaryngoscope and a tracheal tube placed by Boedeker intubation foreceps
Other Names:
  • Aircraft Medical McGRATH series 5 videolaryngoscope
  • Karl Storz Boedeker intubation foreceps

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Time to intubation
Time Frame: within one day
within one day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sore throat
Time Frame: within 2 days
within 2 days
succesful intubation
Time Frame: within one day
within one day
Damage on teeth
Time Frame: 2 days
2 days
Intubation difficulty
Time Frame: within one day
Intubation difficulty scale
within one day
Intubation conditions
Time Frame: within one day
a.m fuchs-buder
within one day
Intubation attempts
Time Frame: within one day
within one day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Camilla Strøm, M.D, Dept. of anaesthesia, centre of head and orthopedics, Rigshospitalet, Denmark

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2013

Primary Completion (ACTUAL)

December 1, 2013

Study Completion (ACTUAL)

December 1, 2013

Study Registration Dates

First Submitted

October 29, 2013

First Submitted That Met QC Criteria

October 29, 2013

First Posted (ESTIMATE)

November 6, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

October 27, 2014

Last Update Submitted That Met QC Criteria

October 24, 2014

Last Verified

October 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • LP-CS-13

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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