EUROpE RSI-Study (EURopean Online Evaluation) - Pan-european Online-survey About Rapid Sequence Induction (RSI) by Anesthetists
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Universitätsklinikum Köln
- Enrollment
- 1,500
- Locations
- 1
- Primary Endpoint
- Differences in the procedure of the RSI (Rapid sequence induction)
Study Overview
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.
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
- Observational Model
- Other
- Time Perspective
- Other
Eligibility Criteria
- Ages
- 25 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Emergency physician
Exclusion Criteria
- •None Emergency physician
Outcomes
Primary Outcomes
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.
Secondary Outcomes
No secondary outcomes reported