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Clinical Trials/NCT05063084
NCT05063084
Recruiting
Phase 3

A Randomised Controlled Trial Comparing Pre-oxygenation Strategies With High-flow Humidified Nasal Oxygenation Versus Apnoeic Facemask Oxygenation During Rapid Sequence Induction in Children Aged Less Then 11 Years

Assistance Publique - Hôpitaux de Paris1 site in 1 country170 target enrollmentFebruary 9, 2023

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Pediatric Surgery
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
170
Locations
1
Primary Endpoint
Intubation without oxygen desaturation episode
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

This randomised study aims to compare the utilization of high-flow humidified nasal oxygenation (HFNO) with standard care, using apnoeic facemask oxygenation, during rapid sequence induction (RSI) of anesthesia in young children.

170 children aged less then 11 years, admitted to the operating room for surgery and with a medical indication of a RSI of anesthesia will be recruited in one university hospital (Necker-Enfants-Malades in Paris).

Children will be randomly assigned into two groups: the control group will benefit of standard care and the HFNO group will receive heated and humidified oxygen through a nasal cannula device during pre-oxygenation and apnoea time prior to tracheal intubation.

HFNO has been evaluated and showed benefits in rapid sequence induction of anesthesia in adults and prolonged apnea time before desaturation in children. To the investigators' knowledge the potential benefit of HFNO during RSI in young children remain to be evaluated.

Detailed Description

Hypoxic events during rapid sequence induction (RSI) in children remain more frequent than during standard induction. Although the exact incidence is difficult to appreciate. However the deleterious consequences of hypoxemia during tracheal intubation procedures are well known. HFNO is an effective technique to supplement oxygen including during apnoea. Studies in children have shown benefits both during breathing and apneic situation. A monocentric controlled randomized study including children, aged less then 11 years, will be conducted in order to assess the potential benefits of this technique during RSI. The rate of successful tracheal intubation without oxygen desaturation is the primary outcome. Children will be randomly assigned into two groups: * The control group will benefit of standard RSI. Pre-oxygenation will be given through facemask with 100% oxygen during 2 minutes, with a flow of 6 to 8 L.min-1 depending on the age of the child. No oxygen will be delivered during laryngoscopy. * The HFNO group will be given 2 L.Kg-1.min-1 of humidified and heated 100% O2 through a nasal cannula during a 2 minutes pre-oxygenation and then throughout laryngoscopy. Adverse events will be recorded and follow-up continued until discharge from the post anesthesia care unit (PACU).

Registry
clinicaltrials.gov
Start Date
February 9, 2023
End Date
September 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • child from birth until 10 years
  • patient needing (elective or in emergency) surgery under general anesthesia requiring tracheal intubation and fulfilling all criteria for a rapid sequence induction
  • Parents or legal guardians signed the Informed consent form
  • Social insurance affiliation
  • Exclusion Criteria
  • child having one or more contraindication to use high flow nasal oxygenation:
  • Nasal obstruction
  • Recent trauma of aero-digestives tracts
  • Epistaxis
  • Known or suspected fracture of the skull base

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Intubation without oxygen desaturation episode

Time Frame: Up to 10 minutes

Intubation without oxygen desaturation episode, defined as pulsed oxymetry \<95% during the rapid sequence induction process of anesthesia in the operating room.

Secondary Outcomes

  • Occurrence of all adverse events(until the exit of the recovery room)
  • Number of attempted tracheal intubations required to succeed the process(Up to 10 minutes)
  • Satisfaction of the anaesthetist and the anaesthesia team regarding the use of HFNO(Exit of the recovery room)
  • Oxygen saturation level(Up to 10 minutes)
  • Tracheal intubation without facemask reventilation(Up to 10 minutes)

Study Sites (1)

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