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FiO2 in Chronic Obstructive Pulmonary Disease (COPD) Patient Normobaric O2 Versus NIV — NIVLEAKS  

COPD Clinical Trial

Official title:
Measured FiO2 With Nasal Canula O2 Versus Noninvasive Ventilation (NIV) With the Same O2 Flow, in COPD Patients the NIV LEAKS Study

Clinical Trial Summary

The purpose of this study is to compare pharyngeal FiO2 in day time with nasal normobaric O2 with inhaled FiO2 in the night time with home care ventilator NIV at the same O2 flow.

Clinical Trial Description

in a prospective observational study the investigators will register FiO2 in 15 voluntaries COPD patients as following:

- Pharyngeal FiO2 (G5® Philips™ side stream FiO2) with O2 supply through nasal cannula at basal flow (flow needed by patient). In order to compare FiO2s the investigators will measure FiO2 with 150%, 75%, 50% and 25 % of basal Flow

- And FiO2 during nocturnal NIV (pressure support ventilation; Vivo 50®, Bréas™), using facial or nasal masque (Confort Gel® Respironics™). O2 flow will be basal flow. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02599246
Study type Observational [Patient Registry]
Source Breas Medical S.A.R.L.
Contact
Status Completed
Phase N/A
Start date November 17, 2015
Completion date February 24, 2016
View Details
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