Rapid Sequence Induction Clinical Trial
— RSIEUOfficial title:
Rapid Sequence Induction in EU: Electronic Survey
NCT number | NCT03694860 |
Other study ID # | RSI 2018 EU |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | July 1, 2019 |
Est. completion date | September 1, 2019 |
Verified date | September 2019 |
Source | Brno University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Rapid sequence induction (RSI) is a common part of routine anesthesiology practice. However several steps of RSI are not based on evidence based data (EBM) and are considered controversial. In an electronic evaluation form that will be send to European Society of Anaesthesiology (ESA) members. The electronic survey will contain 22 question (11 for adult RSI and 11 for paediatric RSI). In the questionnaire the participants will have to describe their routine clinical practice in performing rapid sequence induction.
Status | Completed |
Enrollment | 1921 |
Est. completion date | September 1, 2019 |
Est. primary completion date | September 1, 2019 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - Members of European Society of Anaesthesiology Exclusion Criteria: - not members of ESA |
Country | Name | City | State |
---|---|---|---|
Czechia | University Hospital Brno | Brno |
Lead Sponsor | Collaborator |
---|---|
Brno University Hospital | European Society of Anaesthesiology (ESA) |
Czechia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | RSI practice in European countries - questionnaire (electronic survey) | Evaluation of the clinical practice of the RSI European countries | 2 months |
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