Algorithms in a Simulated Difficult Intubation Scenario

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Aintree University Hospitals NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT00951769
First received: August 3, 2009
Last updated: January 14, 2015
Last verified: August 2009
  Purpose

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.


Condition
Airway Management

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
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

Further study details as provided by Aintree University Hospitals NHS Foundation Trust:

Primary Outcome Measures:
  • Time to safe oxygenation for manikin [ Time Frame: Variable ] [ Designated as safety issue: Yes ]

Enrollment: 30
Study Start Date: March 2009
Study Completion Date: February 2011
Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts
Control,
Control
DAS: Difficult Airway Society, UK
DAS difficult airway algorithm
Australian
Australian difficult airway algorithm

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

Trainee anaesthetists in for 2 years of training

Criteria

Inclusion Criteria:

  • Anaesthetists in first 2 years of training

Exclusion Criteria:

  • Those who decline invitation to participate
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00951769

Locations
United Kingdom
Cheshire & Merseyside Simulation Centre
Liverpool, Merseyside, United Kingdom, L9 7AL
Sponsors and Collaborators
Aintree University Hospitals NHS Foundation Trust
Investigators
Principal Investigator: ARPAN GUHA, MD, FRCA AINTREE HOSPITALS NHS TRUST
  More Information

No publications provided

Responsible Party: Aintree University Hospitals NHS Foundation Trust
ClinicalTrials.gov Identifier: NCT00951769     History of Changes
Other Study ID Numbers: 09/H1001/3
Study First Received: August 3, 2009
Last Updated: January 14, 2015
Health Authority: United Kingdom: Research Ethics Committee

ClinicalTrials.gov processed this record on July 27, 2015