Surgery Clinical Trial
Official title:
Influence of Automatic Oxygen Titration Device (FreeO2) on Percentage of Time Within Oxygen Saturation Target and Induced Hypercapnia During Noninvasive Ventilation for Patients Hospitalized for an Acute Exacerbation of COPD or a Bariatric Surgery
The main objective is to evaluate the FreeO2 device combined with noninvasive respiratory
support technique for COPD patients and postoperative bariatric surgery patients.
The main hypothesis is that FreeO2 device for oxygen therapy associated with NIV or nasal
high flow oxygen therapy (NHFOT) allows to reach better oxygenation and avoid hypoxemia and
hyperoxia.
Bariatric surgery patients:
The main objective of this study is to evaluate the time spent in the SpO2 target (+/- 2%
SpO2 target) and partial pressure of carbon dioxide (PCO2) values on patients with morbid
obesity after bariatric surgery.
COPD patients:
The main objective of this study is to evaluate the time spent in the SpO2 target (+/- 2%
SpO2 target) and PCO2 values on patients with exacerbation of COPD (hypercapnic patients)
with different ventilatory supports (NIV and NHFOT) associated with FreeO2.
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