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NCT00951769 Clinical Trial

Algorithms in a Simulated Difficult Intubation Scenario

Airway Management Clinical Trial

Official title:
A Comparison of the Difficult Airway Society (UK) and Australian Patient Safety Foundation Crisis Algorithms for Difficult Intubation in a Simulated Difficult Intubation Scenario

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00951769
Other study ID # 09/H1001/3
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2009
Est. completion date February 2011

Study information
Verified date August 2009
Source Liverpool University Hospitals NHS Foundation Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a non-human study, conducted in a simulation environment, with simulator manikins, and volunteers from anaesthesia. Trainees in their first 2 years of anaesthetics training will be randomised to a control group, a group following the Difficult Airway Society UK's Guidelines and the Australian Difficult Airway management algorithm. A simulated difficult airway will be created during the induction of anaesthesia. The investigators will examine adherence to guidelines, which would have been provided to participants before the experiment, as well as compare their performance with the guidelines.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date February 2011
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Anaesthetists in first 2 years of training Exclusion Criteria: - Those who decline invitation to participate

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United Kingdom Cheshire & Merseyside Simulation Centre Liverpool Merseyside

Sponsors (1)
Lead Sponsor Collaborator
Liverpool University Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary Time to safe oxygenation for manikin Variable
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