The objective of our study is to carry out an evaluation of the safety and the effectiveness of the use of the MakAir respirator as useful supplement in situation of shortage of technical devices of assistance to the mechanical invasive ventilation, related to COVID-19 through a protocol in 3 successive sequences.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
4
MakAir artificial ventilator
CHRU Brest
Brest, Finistère, France
CHU Nantes
Nantes, Loire-Atlantique, France
Number of dysfunctions
Number of dysfunctions which can lead to or have led to "respiratory" adverse events or to serious adverse events (SAE)
Time frame: 24 hours for sequence 1
Number of dysfunctions
Number of dysfunctions which can lead to or have led to "respiratory" adverse events or to serious adverse events (SAE)
Time frame: 5 days for sequence 2
Number of dysfunctions
Number of dysfunctions which can lead to or have led to "respiratory" adverse events or to serious adverse events (SAE)
Time frame: 10 days for sequence 3
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