NCT04126356

Brief Summary

Check the intubation conditions during laryngoscopy without external mobilization of the larynx, with Sellick manoeuvre or with low paratracheal esophagal compression.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
45

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

February 1, 2019

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 12, 2019

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 29, 2019

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

October 11, 2019

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 15, 2019

Completed
Last Updated

October 15, 2019

Status Verified

October 1, 2019

Enrollment Period

2 months

First QC Date

October 11, 2019

Last Update Submit

October 14, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • Distance between oesophagus and trachea

    Distance between oesophagus and trachea

    During laryngoscopy procedure

Interventions

Check the intubation conditions during laryngoscopy without external mobilization of the larynx, with Sellick manoeuvre or with low paratracheal esophagal compression.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults patients undergoing general anaesthesia

You may qualify if:

  • Adults patients undergoing general anaesthesia

You may not qualify if:

  • pregnant women
  • people with facial
  • oropharyngeal abnormalities

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Liege, University Hospital

Liège, 4000, Belgium

Location

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

October 11, 2019

First Posted

October 15, 2019

Study Start

February 1, 2019

Primary Completion

April 12, 2019

Study Completion

September 29, 2019

Last Updated

October 15, 2019

Record last verified: 2019-10

Locations