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EUROpE-RSI (EURopean Online Evaluation RSI Study)

Sponsor
Universitätsklinikum Köln (Other)
Overall Status
Completed
CT.gov ID
NCT02751684
Collaborator
(none)
1,500
Enrollment
1
Location
3
Actual Duration (Months)
501.7
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The investigators want to identify and show differences in standards and procedures of in-hospital rapid sequence induction by collecting data with an online survey for anaesthetist in Europe.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The study is designed as a web-based online survey for anaesthetist in Europe. They will be invited via mail, as members of the European Society of Anaesthesiology (ESA), the participation is voluntary.

    The survey contains 30 items about the standards and procedures of in-hospital rapid sequence induction (RSI). There will be a selection of possible answers, only a few items contains free-text answers.

    The study collects only personal data to age, country, gender and level of training.

    The collected data should identify differences in the procedures of RSI.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    1500 participants
    Observational Model:
    Other
    Time Perspective:
    Other
    Official Title:
    EUROpE RSI-Study (EURopean Online Evaluation) - Pan-european Online-survey About Rapid Sequence Induction (RSI) by Anesthetists
    Actual Study Start Date :
    Mar 1, 2017
    Actual Primary Completion Date :
    May 31, 2017
    Actual Study Completion Date :
    May 31, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Differences in the procedure of the RSI (Rapid sequence induction) [04.30.2016-10.30.2016]

      The questionnaire date will be collected up to 6 month and processed with Microsoft Excel.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Emergency physician
    Exclusion Criteria:
    • None Emergency physician

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University hospital of Cologne Cologne NRW Germany 50935

    Sponsors and Collaborators

    • Universitätsklinikum Köln

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Universitätsklinikum Köln
    ClinicalTrials.gov Identifier:
    NCT02751684
    Other Study ID Numbers:
    • UKoln
    First Posted:
    Apr 26, 2016
    Last Update Posted:
    Apr 4, 2019
    Last Verified:
    Apr 1, 2019
    Keywords provided by Universitätsklinikum Köln
    Rapid Sequence Induction
    European
    Evaluation
    EUROpE RSI
    Standards
    RSI

    Study Results

    No Results Posted as of Apr 4, 2019