Clinical Trials Directory

Trials / Completed

CompletedNCT02167334

Using Positive Pressure Ventilation for Preoxygenation During Panendoscopy.

Non Invasive Ventilation (NIV) Versus Spontaneous Breathing for Preoxygenation During Ear, Nose, and Throat (ENT) Panendoscopy. A Controlled, Prospective, Randomized Study.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Centre Hospitalier Universitaire, Amiens · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

the aim of the study is to determine if Spontaneous Ventilation with Positive Pressure Ventilation (PPV) preoxygenation allows a longer non hypoxemic apnea time during panendoscopy compared to spontaneous breathing preoxygenation. the hypothesis is PPV extends the residual functional capacity of lung so it provides more oxygen during apnea.

Conditions

Interventions

TypeNameDescription
DEVICEpositive pressure ventilationPositive Pressure Ventilation with a 4 cmH2O inhale pressure, a positive end-expiratory pressure of 4 cm H2O, a trigger 2, an inspiratory slope of 0, an inhaled oxygen fraction of 100% administered at a 10 L / min flow.
PROCEDUREOxygenation with simple breathing maskSpontaneously breathing preoxygenation with adapted face mask, to restrict leakage, at 10L/min oxygen, with inhaled fraction of 100% and a 2 L balloon volume.

Timeline

Start date
2013-09-01
Primary completion
2013-09-01
Completion
2014-06-01
First posted
2014-06-19
Last updated
2025-09-22

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02167334. Inclusion in this directory is not an endorsement.