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Procedural Simulation for Difficult Airway Training in Anesthesiology Resident Education Program (PROSIDIAIR)

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ClinicalTrials.gov Identifier: NCT02470195
Recruitment Status : Completed
First Posted : June 12, 2015
Last Update Posted : July 7, 2016
Sponsor:
Information provided by (Responsible Party):
Lilot Marc, Claude Bernard University

Brief Summary:
Difficult airway management is a crucial point that may influence outcomes of patient in this critical situation. Education for this topic is of main importance for resident of anesthesiology. Procedural simulation workshop allows participant to use device dedicated to difficult airway management. Investigators included this workshop to a state education program of anesthesiology resident in second year and compared to their homonym in another state where no specific organized workshop is integrated to the education program.

Condition or disease Intervention/treatment Phase
Behaviour Behavioral: workshop Not Applicable

Detailed Description:
Difficult airway management is a crucial point that may influence outcome of patient in this critical situation. Education for this topic is of main importance for resident of anesthesiology. Procedural simulation workshop allows participant to use device dedicated to difficult airway management. The investigators included this workshop for smal groups of 6-10 anesthesiology resident from Rhône Alpes Auvergne french state. Participants were ask to fill out a questionnaire about their specific knowledge and experience of several devices usable in difficult airway management situation. The workshop was a small briefing as an introduction to the workshop and then small workshop of 20-45 min for specific procedural use of different devices for difficult airway management : Eischmann guide, LMA, supraglottic devices, fiberoptic with spontaneous breathing, cricothyroidotomy, jet ventilation, percutaneous tracheotomy... Investigator will compare at 6 month the incidence of use of the difficult airway devices between resident from rhone alpes auvergne following the workshop and resident from Montpellier that did not follow specific organized workshop.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 60 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Official Title: Anesthesiology Education Implementation by Procedural Simulation Workshop for Difficult Airway Management: a Controlled Interregional French Study
Study Start Date : November 2014
Actual Primary Completion Date : June 2016
Actual Study Completion Date : June 2016

Arm Intervention/treatment
Experimental: workshop
workshop of procedural simulation
Behavioral: workshop
workshop for procedural simulation for education in difficult airway situation

No Intervention: control
no specific workshop of procedural simulation



Primary Outcome Measures :
  1. incidence of use of airway devices between groups [ Time Frame: 6 month ]
    modification in the incidence of use of airway devices between workshop and control groups


Secondary Outcome Measures :
  1. confidence with airway device [ Time Frame: 6 month ]
    questionnaire of confidence with the usability of the devices. Scale from 0 to 10.



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Residents in 2nd year of anesthesiology residency in Rhones alpes auvergne and in Nîmes

Exclusion Criteria:

  • Exclusion demand from the participant

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02470195


Locations
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France
CLESS
Lyon, Rhône-Alpes, France, 69007
Sponsors and Collaborators
Claude Bernard University
Investigators
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Principal Investigator: marc Lilot, MD CLESS
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Lilot Marc, MD, Claude Bernard University
ClinicalTrials.gov Identifier: NCT02470195    
Other Study ID Numbers: CLESS PROSIDIAIR 2014
First Posted: June 12, 2015    Key Record Dates
Last Update Posted: July 7, 2016
Last Verified: July 2016
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: data will be analysed by group, no plan to share data has been programmed