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Trial record 1 of 1 for:    Europe rsi
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EUROpE-RSI (EURopean Online Evaluation RSI Study) (EUROpE-RSI)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02751684
Recruitment Status : Completed
First Posted : April 26, 2016
Last Update Posted : April 4, 2019
Sponsor:
Information provided by (Responsible Party):
Universitätsklinikum Köln

Study Description
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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
Rapid Sequence Induction

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
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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 : March 1, 2017
Actual Primary Completion Date : May 31, 2017
Actual Study Completion Date : May 31, 2017
Groups and Cohorts
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Outcome Measures
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Primary Outcome Measures :
  1. Differences in the procedure of the RSI (Rapid sequence induction) [ Time Frame: 04.30.2016-10.30.2016 ]
    The questionnaire date will be collected up to 6 month and processed with Microsoft Excel.


Eligibility Criteria
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Information from the National Library of Medicine

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, Learn About Clinical Studies.


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Ages Eligible for Study:   25 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Emergency physicians from europe; e.g. members of the European Society of Anaestesiology
Criteria

Inclusion Criteria:

  • Emergency physician

Exclusion Criteria:

  • None Emergency physician
Contacts and Locations
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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): NCT02751684


Locations
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Germany
University hospital of Cologne
Cologne, NRW, Germany, 50935
Sponsors and Collaborators
Universitätsklinikum Köln
More Information
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Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
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Responsible Party: Universitätsklinikum Köln
ClinicalTrials.gov Identifier: NCT02751684    
Other Study ID Numbers: UKoln
First Posted: April 26, 2016    Key Record Dates
Last Update Posted: April 4, 2019
Last Verified: April 2019
Keywords provided by Universitätsklinikum Köln:
Rapid Sequence Induction
European
Evaluation
 EUROpE RSI
Standards
RSI