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OpenTrials
Completed

NCT Number: NCT02786355

Oxygenation Via Frova Bougie and Ambu Bag

We will conduct this study to show that it is possible to deliver air through a Frova bougie and an Ambu® bag.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

BC Women's Hospital

Vancouver, British Columbia, V5X1T3, Canada

About this study

Participants will be invited to squeeze an Ambu® bag connected to a Frova bougie, and we will measure the volume of air delivered and peak pressure generated.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • staff, fellows and resident anesthesiologists

Exclusion criteria

  • injury to hand

Treatment and study plan

Frova bougie

Other

Squeezing an Ambu bag and delivering air through a Frova bougie. Measuring mean volumes of air delivered and peak pressures generated.

Primary outcomes

  1. Tidal Volume (ml)

    Time frame: 15 minutes

    volume of air delivered via Frova bougie (milliliters)

Sponsors and collaborators

Lead sponsor

University of British Columbia

Other

Registry information

Official study title

Comparison of Volumes of Air Delivered Through a Frova Intubation Bougie by a Maximal Bimanual Compression Versus a Normal Bimanual Compression of an Adult Ambu® Bag

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Jun 1, 2016
Registry last updated
Dec 28, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.