Name (Synonyms) | Correlation | |
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drug1781 | Pectin Wiki | 1.00 |
drug2080 | Respiratory Mechanics Wiki | 1.00 |
drug106 | Acacia Senegal Wiki | 1.00 |
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.
This is a multicenter randomized controlled clinical trial with adaptive design assessing the efficacy of setting the ventilator based on measurements of respiratory mechanics (recruitability and effort) to reduce Day 60 mortality in patients with acute respiratory distress syndrome (ARDS)
Description: The lack of an appropriate surrogate endpoint, and the high baseline mortality rate mandate a multicentre RCT to determine the mortality effects of setting the ventilator based on recruitability and effort compared with conventional ventilation.
Measure: All-cause 60-day mortality Time: 60 daysDescription: Organ dysfunction as per the SOFA score
Measure: Number of patients with organ dysfunction Time: Day 1-7, 14, 21, 28Description: Barotrauma defined as new onset of pneumothorax
Measure: Number of patients with barotrauma Time: Up to 60 daysDescription: Biomarkers include interleukin 6 (IL-6), interleukin 8 (IL-8), tumor necrosis factor receptor 1 (TNFr1), soluble receptor of the advanced glycation end products (sRAGE), and surfactant protein D (SPD). All measured in pg/ml
Measure: The change in biomarker expression Time: Baseline, 24 and 72 hours