CompletedPhase 2ACTRN12617000339358

End-tidal oxygen achieved with preoxygenation via non-rebreather mask at different flow rates in healthy volunteers

Efficacy of preoxygenation via non-rebreather mask, comparing standard oxygen flow at 15lpm to maximally opened flow meter in healthy participants


Sponsor

NSW Ambulance

Enrollment

40 participants

Start Date

Mar 1, 2016

Study Type

Interventional

Conditions

Summary

Preoxygenation is critical to safe emergency airway management. Outside of the operating theatre and in prehospital environments, ‘Over flow’ from a standard wall/cylinder outlet has been proposed to greatly enhance preoxygenation via a Non-rebreather mask (NRB). Methods We performed a randomised crossover trial using two preoxygenation conditions; a NRB at 15lpm and the other a NRB with the 15lpm flowmeter with the dial turned all the way open (over-flow). End-tidal oxygen (ETO2) as a measure of preoxygenation/denitrogenating efficacy, was measured by single exhaled vital capacity breath.


Eligibility

Sex: Both males and femalesMin Age: 16 YearssMax Age: 70 Yearss

Inclusion Criteria2

  • No regular cardiovascular or respiratory medication, no history of chronic respiratory disease.
  • Attendees at NSW Ambulance Aeromedical service governance days. We are not allowed to recruit outside of this site.

Exclusion Criteria3

  • Pregnancy, lung disease, known or suspected coronary or cerebrovascular disease, treatment for asthma or
  • COPD, previous exposure to bleomycin, participants with beards, dentures or facial abnormalities affecting mask
  • seal.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

The study design is two-period crossover study (repeated measures design) . Participants will complete two trials of 3-minutes pre-oxygenation via non-rebreather mask (NRM)., One trial will have an ox

The study design is two-period crossover study (repeated measures design) . Participants will complete two trials of 3-minutes pre-oxygenation via non-rebreather mask (NRM)., One trial will have an oxygen flow rate of 15lpm, The other will have the flow-meter valve turned wide open. The end-tidal oxygen (ETO2) will be measured at the end of each trial. The first trial will be followed by a washout period of 2 minutes. Allocation to the first trial (15lpm or fully open valve) will be randomised.


Locations(1)

NSW, Australia

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12617000339358


Related Trials