EUROpE-RSI (EURopean Online Evaluation RSI Study)

Rapid Sequence Induction Clinical Trial

— EUROpE-RSI  

Official title:

EUROpE RSI-Study (EURopean Online Evaluation) - Pan-european Online-survey About Rapid Sequence Induction (RSI) by Anesthetists

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02751684
• Other study ID #: UKoln
• Status: Completed
• Start date: March 1, 2017
• Est. completion date: May 31, 2017

Study information

• Verified date: April 2019
• Source: Universitätsklinikum Köln
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1500
• Est. completion date: May 31, 2017
• Est. primary completion date: May 31, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 25 Years to 70 Years

Eligibility

Inclusion Criteria:

• Emergency physician

Exclusion Criteria:

• None Emergency physician

Related Conditions & MeSH terms

• Rapid Sequence Induction

Locations

Country	Name	City	State
Germany	University hospital of Cologne	Cologne	NRW

Sponsors (1)

Lead Sponsor	Collaborator
Universitätsklinikum Köln

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Differences in the procedure of the RSI (Rapid sequence induction)	The questionnaire date will be collected up to 6 month and processed with Microsoft Excel.	04.30.2016-10.30.2016