EUROpE-RSI (EURopean Online Evaluation RSI Study)

Completed

• Conditions: Rapid Sequence Induction

• Registration Number: NCT02751684
• Lead Sponsor: Universitätsklinikum Köln

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 Timeline

• Study First Submitted: 2016-04-11
• Study First Submitted QC: 2016-04-25
• Study First Posted: 2016-04-26
• Study Start: 2017-03-01
• Primary Completion: 2017-05-31
• Study Completion: 2017-05-31
• Status Verified: 2019-04
• Last Update Submitted: 2019-04-03
• Last Update Posted: 2019-04-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 1500

Inclusion Criteria

• Emergency physician

Exclusion Criteria

• None Emergency physician

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.

Trial Locations

Locations (1)

University hospital of Cologne; 🇩🇪 Cologne, NRW, Germany