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Clinical Trial Summary

Airway management is a core clinical skill in anaesthesia. Pre-oxygenation prior to induction of anaesthesia is standard practice to prevent desaturation. Apnoeic oxygenation in adults is effective and prolongs the time to desaturation. The effectiveness of apnoeic oxygenation in the adult is well document, however evidence in the paediatric is lacking. Therefore, the aim of this study was to investigate the effectiveness of apnoeic oxygenation during airway management in children.

This was a pilot randomised controlled trial. Patients were randomised to either receive apnoeic oxygenation or standard care during the induction of anaesthesia. The primary outcome was the duration of safe apnoea, defined as a composite of the time to first event, either time for SpO2 to drop to 92% or time to successfully secure the airway, and the lowest SpO2 observed during airway management. Secondary outcomes were number of patients whose SpO2 dropped below 95% and number of patients whose SpO2 dropped below 92%.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03271827
Study type Interventional
Source University of Birmingham
Contact
Status Completed
Phase N/A
Start date January 2016
Completion date July 2016

See also
  Status Clinical Trial Phase
Completed NCT03478774 - Physiology Regarding Apnoeic Oxygenation During Nasal Cannula Therapy at Different Flow Rates N/A
Completed NCT03738722 - Positive Airway Pressure Under Apnoeic Oxygenation With Different Flow Rates in Nasal Cannula Therapy N/A