Name (Synonyms) | Correlation | |
---|---|---|
D055371 | Acute Lung Injury NIH | 0.10 |
D012127 | Respiratory Distress Syndrome, Newborn NIH | 0.10 |
D012128 | Respiratory Distress Syndrome, Adult NIH | 0.09 |
Name (Synonyms) | Correlation |
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There is one clinical trial.
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.
Description: Number of dysfunctions which can lead to or have led to "respiratory" adverse events or to serious adverse events (SAE)
Measure: Number of dysfunctions Time: 24 hours for sequence 1Description: Number of dysfunctions which can lead to or have led to "respiratory" adverse events or to serious adverse events (SAE)
Measure: Number of dysfunctions Time: 5 days for sequence 2Description: Number of dysfunctions which can lead to or have led to "respiratory" adverse events or to serious adverse events (SAE)
Measure: Number of dysfunctions Time: 10 days for sequence 3