EUROpE-RSI (EURopean Online Evaluation RSI Study)

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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02751684

Acronym

EUROpE-RSI

Enrollment

1500

Registered

2016-04-26

Start date

2017-03-01

Completion date

2017-05-31

Last updated

2019-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rapid Sequence Induction

Keywords

Rapid Sequence Induction, European, Evaluation, EUROpE RSI, Standards, RSI

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.

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

OTHER

Eligibility

Sex/Gender

ALL

Age

25 Years to 70 Years

Healthy volunteers

Inclusion criteria

* Emergency physician

Exclusion criteria

* None Emergency physician

Design outcomes

Primary

Measure	Time frame	Description
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.

Countries

Germany

Outcome results