Condition or disease | Intervention/treatment |
---|---|
Rapid Sequence Induction | Other: questionnaire |
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.
The 11 will be consulted with the research committee of ESA.
Study Type : | Observational |
Actual Enrollment : | 1921 participants |
Observational Model: | Other |
Time Perspective: | Prospective |
Official Title: | Rapid Sequence Induction in EU: Electronic Survey |
Actual Study Start Date : | July 1, 2019 |
Actual Primary Completion Date : | September 1, 2019 |
Actual Study Completion Date : | September 1, 2019 |
Tracking Information | |||||
---|---|---|---|---|---|
First Submitted Date | October 2, 2018 | ||||
First Posted Date | October 3, 2018 | ||||
Last Update Posted Date | September 13, 2019 | ||||
Actual Study Start Date | July 1, 2019 | ||||
Actual Primary Completion Date | September 1, 2019 (Final data collection date for primary outcome measure) | ||||
Current Primary Outcome Measures |
RSI practice in European countries - questionnaire (electronic survey) [ Time Frame: 2 months ] Evaluation of the clinical practice of the RSI European countries
|
||||
Original Primary Outcome Measures | Same as current | ||||
Change History | |||||
Current Secondary Outcome Measures | Not Provided | ||||
Original Secondary Outcome Measures | Not Provided | ||||
Current Other Pre-specified Outcome Measures | Not Provided | ||||
Original Other Pre-specified Outcome Measures | Not Provided | ||||
Descriptive Information | |||||
Brief Title | Rapid Sequence Induction EU: Electronic Survey (RSIEU) | ||||
Official Title | Rapid Sequence Induction in EU: Electronic Survey | ||||
Brief Summary | 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. | ||||
Detailed Description |
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. The 11 will be consulted with the research committee of ESA. |
||||
Study Type | Observational | ||||
Study Design | Observational Model: Other Time Perspective: Prospective |
||||
Target Follow-Up Duration | Not Provided | ||||
Biospecimen | Not Provided | ||||
Sampling Method | Non-Probability Sample | ||||
Study Population | Members of Europen Society of Anaesthesiology | ||||
Condition | Rapid Sequence Induction | ||||
Intervention | Other: questionnaire
Members of European society of anaesthesiology care will obtain an electronic survey considering their clinical practice in RSI
Other Name: electronic survey
|
||||
Study Groups/Cohorts | Not Provided | ||||
Publications * | Klucka J, Kosinova M, Zacharowski K, De Hert S, Kratochvil M, Toukalkova M, Stoudek R, Zelinkova H, Stourac P. Rapid sequence induction: An international survey. Eur J Anaesthesiol. 2020 Jun;37(6):435-442. doi: 10.1097/EJA.0000000000001194. | ||||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
|||||
Recruitment Information | |||||
Recruitment Status | Completed | ||||
Actual Enrollment |
1921 | ||||
Original Estimated Enrollment |
500 | ||||
Actual Study Completion Date | September 1, 2019 | ||||
Actual Primary Completion Date | September 1, 2019 (Final data collection date for primary outcome measure) | ||||
Eligibility Criteria |
Inclusion Criteria: - Members of European Society of Anaesthesiology Exclusion Criteria: - not members of ESA |
||||
Sex/Gender |
|
||||
Ages | 18 Years to 99 Years (Adult, Older Adult) | ||||
Accepts Healthy Volunteers | Not Provided | ||||
Contacts | Contact information is only displayed when the study is recruiting subjects | ||||
Listed Location Countries | Czechia | ||||
Removed Location Countries | |||||
Administrative Information | |||||
NCT Number | NCT03694860 | ||||
Other Study ID Numbers | RSI 2018 EU | ||||
Has Data Monitoring Committee | No | ||||
U.S. FDA-regulated Product |
|
||||
IPD Sharing Statement |
|
||||
Responsible Party | Petr Štourač, MD, Brno University Hospital | ||||
Study Sponsor | Brno University Hospital | ||||
Collaborators | European Society of Anaesthesiology (ESA) | ||||
Investigators |
|
||||
PRS Account | Brno University Hospital | ||||
Verification Date | September 2019 |