- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02470195
Procedural Simulation for Difficult Airway Training in Anesthesiology Resident Education Program (PROSIDIAIR)
July 5, 2016 updated by: Lilot Marc, Claude Bernard University
Anesthesiology Education Implementation by Procedural Simulation Workshop for Difficult Airway Management: a Controlled Interregional French Study
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.
Study Overview
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.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
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
-
-
Rhône-Alpes
-
Lyon, Rhône-Alpes, France, 69007
- CLESS
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Residents in 2nd year of anesthesiology residency in Rhones alpes auvergne and in Nîmes
Exclusion Criteria:
- Exclusion demand from the participant
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
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: workshop
workshop of procedural simulation
|
workshop for procedural simulation for education in difficult airway situation
|
|
No Intervention: control
no specific workshop of procedural simulation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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
|
6 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
confidence with airway device
Time Frame: 6 month
|
questionnaire of confidence with the usability of the devices.
Scale from 0 to 10.
|
6 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
November 1, 2014
Primary Completion (Actual)
June 1, 2016
Study Completion (Actual)
June 1, 2016
Study Registration Dates
First Submitted
May 28, 2015
First Submitted That Met QC Criteria
June 9, 2015
First Posted (Estimate)
June 12, 2015
Study Record Updates
Last Update Posted (Estimate)
July 7, 2016
Last Update Submitted That Met QC Criteria
July 5, 2016
Last Verified
July 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- CLESS PROSIDIAIR 2014
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
data will be analysed by group, no plan to share data has been programmed
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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