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CompletedNCT02751684EUROpE-RSIUpdated Apr 4, 2019

EUROpE-RSI (EURopean Online Evaluation RSI Study)

An observational study in Rapid Sequence Induction, sponsored by Universitätsklinikum Köln. Completed at 1 site in Germany. Open to participants aged 25 Years to 70 Years. Per ClinicalTrials.gov, last updated 2019-04-04.

Sponsored by Universitätsklinikum Köln · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
1,500
Ages
25 Years to 70 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Rapid Sequence Induction

Keywords

  • Rapid Sequence Induction
  • European
  • Evaluation
  • EUROpE RSI
  • Standards
  • RSI
03

In context

Lead sponsor

Universitätsklinikum Köln is the lead sponsor of 31 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Emergency physicians from europe; e.g. members of the European Society of Anaestesiology

Inclusion criteria

  • Emergency physician

Exclusion criteria

Exclusion Criteria:

  • None Emergency physician
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
1,500 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: 04.30.2016-10.30.2016

07

Study locations

1 site
  • University hospital of Cologne
    Cologne, NRW 50935, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02751684
Lead sponsor
Universitätsklinikum Köln
Responsible party
Sponsor
First posted
Apr 26, 2016
Start date
Mar 1, 2017
Primary completion
May 31, 2017
Completion
May 31, 2017
Last update
Apr 4, 2019

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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