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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02985970
Other study ID # RSI 2016CZ
Secondary ID
Status Completed
Phase N/A
First received November 30, 2016
Last updated April 21, 2017
Start date December 2016
Est. completion date April 2017

Study information

Verified date April 2017
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 Czech society of anesthesiology, resuscitation and intensive care (ČSARIM) members, the investigators bring 4 clinical scenarios in which RSI should be used. In the questionnaire the participants have to choose RSI or no and they have to describe all the next steps on anesthesia induction process in each single clinical scenario.


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 Czech society of anesthesiology, resuscitation and intensive care (ČSARIM) members, the investigators bring 4 clinical scenarios in which RSI should be used. In the questionnaire the participants have to choose RSI or no and they have to describe all the next steps on anesthesia induction process in each single clinical scenario.

- 1st. scenario - adult patient with acute abdomen in the OR to be anesthetized

- 2nd. scenario - 4 years old child with acute abdomen in the OR scheduled for an acute surgery

- 3rd. scenario - pregnant women scheduled for an elective caesarean section in the OR

- 4th. scenario - geriatric patient with hiatal hernia scheduled for an elective laparoscopic cholecystectomy.

In each scenario the several steps of the RSI sequence has to be answered:

Is RSI indicated? Y N

Peripheral vein line before induction? Y N

Nasogastric tube before/after induction or without?

Patients position: neutral, head-up, head-down?

Preoxygenation - 3/5minutes, breaths, (CPAP)/Positive end-expiratory pressure (PEEP)?

Sellick manoeuver? Y N

Drugs for induction (order with the number in the row) - propofol, etomidate, ketamine, thiopental, midazolam, suxamethonium, rocuronium, cisatracurium, atracurium, vecuronium

Manual hand-bag ventilation after induction: with limited pressure/contraindicated

Airway: tracheal tube with the cuff/without cuff/laryngeal mask

Comments


Recruitment information / eligibility

Status Completed
Enrollment 164
Est. completion date April 2017
Est. primary completion date February 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 80 Years
Eligibility Inclusion Criteria:

- all members of CSARIM and www.akutne.cz

Exclusion Criteria:

- not members of CSARIM and www.akutne.cz

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaire
The questionnaire will be send to all members of CSARIM with the selected 4 controversial clinical scenarios in which the RSI should be used

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Brno University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary RSI practice in Czech Republic - questionnaire Evaluation of the clinical practice of the RSI in Czech Republic one month
See also
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Not yet recruiting NCT05067829 - Rapid Sequence Intubation With Rocuronium in Elderly Patients N/A
Completed NCT03694860 - Rapid Sequence Induction EU: Electronic Survey (RSIEU)
Recruiting NCT05063084 - High-flow Nasal Cannula Oxygenation During Rapid Sequence Induction in Children Phase 3