Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date September 2019
Source Brno University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaire
Members of European society of anaesthesiology care will obtain an electronic survey considering their clinical practice in RSI

Locations

Country Name City State
Czechia University Hospital Brno Brno

Sponsors (2)

Lead Sponsor Collaborator
Brno University Hospital European Society of Anaesthesiology (ESA)

Country where clinical trial is conducted

Czechia, 

Outcome

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
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT04709315 - Rapid Sequence Induction: Succinyl Choline vs Rocuronium After Pretreatment With Dexmedetomidine Phase 3
Recruiting NCT05775029 - RSI Observation Follow-up
Terminated NCT05384665 - Impact of Opioids on Heart Rate During Rapid Sequence Intubation N/A
Completed NCT04312425 - Classic and Modified Rapid Sequence Induction for Prevention of Gastric Content Regurgitation
Completed NCT02751684 - EUROpE-RSI (EURopean Online Evaluation RSI Study)
Completed NCT04926337 - Preoxygenation With High-flow Nasal Oxygen in Adult Trauma Patients During Rapid Sequence Induction Anaesthesia
Not yet recruiting NCT05067829 - Rapid Sequence Intubation With Rocuronium in Elderly Patients N/A
Recruiting NCT05063084 - High-flow Nasal Cannula Oxygenation During Rapid Sequence Induction in Children Phase 3
Completed NCT02985970 - Rapid Sequence Induction Czech Republic: Survey N/A