Completed

Impact of Cricoid Pressure and BURP on Airway Dimensions

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Study Aim

This study aims to observe how cricoid pressure and the BURP maneuver affect the dimensions of your airway.

What is being collected

Data Collection

Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: June 2011
See protocol details

Summary

Principal SponsorCatharina Ziekenhuis Eindhoven
Last updated: September 7, 2012
Sourced from a government-validated database.Claim as a partner

Study start date: June 1, 2011

Actual date on which the first participant was enrolled.

Cricoid pressure (CP) and the backward-upward-rightward pressure (BURP) manoeuver, are extralaryngeal manoeuvers which are widely applied during endotracheal intubation, respectively offering potential protection against passive gastric regurgitation and improved laryngeal view in emergency airway management. Their validity in achieving an improvement of the laryngeal view has been questioned. The objective of this study is to measure the change in mean anterior-posterior rima glottidis (APRIMA) distance and mean area under the vocal cords after backward upward rightward pressure (BURP) and cricoid pressure (CP). The investigators will measure the APRIMA distances and areas under the vocal cords, using a specially created module in the program DeVIDE. The measurements assessed during BURP and CP will be expressed relative to the measurements when no external pressure is applied.

Principal SponsorCatharina Ziekenhuis Eindhoven
Last updated: September 7, 2012
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

200 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: - 200 consecutive adult patients scheduled for elective surgery requiring endotracheal intubation Exclusion Criteria: BMI > 35 kg.m-2); chronic obstructive pulmonary disease; history of difficult intubation; mouth opening < 3 cm; inadequate neck mobility; history of oropharyngeal pathology.

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Catharina Hospital

Eindhoven, NetherlandsOpen Catharina Hospital in Google Maps
CompletedOne Study Center