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
- Study Details
- Tabular View
- No Results Posted
- How to Read a Study Record
|Condition or disease|
|Rapid Sequence Induction|
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 Type :||Observational|
|Actual Enrollment :||1500 participants|
|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|
- 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.
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.
|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|
- Emergency physician
- None Emergency physician
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
|University hospital of Cologne|
|Cologne, NRW, Germany, 50935|
|Responsible Party:||Universitätsklinikum Köln|
|Other Study ID Numbers:||
|First Posted:||April 26, 2016 Key Record Dates|
|Last Update Posted:||April 4, 2019|
|Last Verified:||April 2019|
Rapid Sequence Induction