Oxygenation Via Frova Bougie and Ambu Bag

Failed or Difficult Intubation Clinical Trial

Official 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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02786355
• Other study ID #: H15-03391
• Status: Completed
• Phase: N/A
• Start date: February 2016
• Est. completion date: March 2016

Study information

• Verified date: June 2018
• Source: University of British Columbia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• staff, fellows and resident anesthesiologists

Exclusion Criteria:

• injury to hand

Related Conditions & MeSH terms

• Failed or Difficult Intubation

Intervention

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

Locations

Country	Name	City	State
Canada	BC Women's Hospital	Vancouver	British Columbia

Sponsors (1)

Lead Sponsor	Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tidal Volume (ml)	volume of air delivered via Frova bougie (milliliters)	15 minutes