Clinical Trials Directory

Trials / Completed

CompletedNCT02599246

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

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

Status
Completed
Phase
Study type
Observational
Enrollment
14 (actual)
Sponsor
Breas Medical S.A.R.L. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2015-11-17
Primary completion
2016-02-22
Completion
2016-02-24
First posted
2015-11-06
Last updated
2017-02-01

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02599246. Inclusion in this directory is not an endorsement.

FiO2 in Chronic Obstructive Pulmonary Disease (COPD) Patient Normobaric O2 Versus NIV (NCT02599246) · Clinical Trials Directory