- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01976546
Intubation With McGrath Video Laryngoscope and Boedeker Intubation Foreceps in a Population of Patients With Predictors of Difficult Airway
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
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Copenhagen, Denmark, 2100
- Dept. of Anaesthesia, Centre of Head and Orthopedics 4231, Rigshospitalet
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
airway
Patients with one or more predictors of diffucult airway
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Patients will be intubated with the Mcgrath videolaryngoscope and a tracheal tube placed by Boedeker intubation foreceps
Other Names:
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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
|
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Damage on teeth
Time Frame: 2 days
|
2 days
|
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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
Sponsor
Investigators
- Principal Investigator: Camilla Strøm, M.D, Dept. of anaesthesia, centre of head and orthopedics, Rigshospitalet, Denmark
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
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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