NCT04206111

Brief Summary

Check in gastric ultrasound for lack of stomach insufflation during preoxygenation with high-flow nasal cannulas

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 15, 2019

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 20, 2019

Completed
5 months until next milestone

Study Start

First participant enrolled

June 1, 2020

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2020

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2020

Completed
Last Updated

June 16, 2020

Status Verified

June 1, 2020

Enrollment Period

3 months

First QC Date

December 15, 2019

Last Update Submit

June 15, 2020

Conditions

Gastric Ultrasound

Outcome Measures

Primary Outcomes (1)

  • no gastric insufflation

    Number of Participants with no gastric insufflation

    From date of randomization until the date of first documented progression, whichever came first, assessed up to 6 months

Study Arms (1)

Preoxygenation

Procedure: Preoxygenation

Interventions

PreoxygenationPROCEDURE

preoxygenation with high flow nasal cannula at 40l/min for 5min

Preoxygenation

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults

You may qualify if:

  • Adults Volunteers

You may not qualify if:

  • History of gastric surgery
  • Facial or oropharyngeal abnormality

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Javillier

Liège, 4000, Belgium

RECRUITING

Central Study Contacts

Benjamin Javillier, MD

CONTACT

003243667180benjamin.javillier@chuliege.be

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 15, 2019

First Posted

December 20, 2019

Study Start

June 1, 2020

Primary Completion

September 1, 2020

Study Completion

October 1, 2020

Last Updated

June 16, 2020

Record last verified: 2020-06

Locations

BE(1)