Developed by Shray Alag, The Harker School
Sections: Correlations,
Clinical Trials, and HPO
Navigate: Clinical Trials and HPO
| Name (Synonyms) | Correlation | |
|---|---|---|
| drug341 | Aprepitant injectable emulsion Wiki | 1.00 |
| drug3505 | Saline Placebo Wiki | 0.58 |
| Name (Synonyms) | Correlation | |
|---|---|---|
| D012127 | Respiratory Distress Syndrome, Newborn NIH | 0.08 |
| D055371 | Acute Lung Injury NIH | 0.08 |
| D012128 | Respiratory Distress Syndrome, Adult NIH | 0.07 |
| Name (Synonyms) | Correlation |
|---|
Navigate: Correlations HPO
There is one clinical trial.
The purpose of this study is to evaluate if a postural recruitment maneuver (PRM) improves the aeration and distribution of lung ventilation in patients with Acute Respiratory Distress Syndrome (ARDS) caused by COVID-19 infection; without the need to reach high airway pressures as in the standard lung recruitment maneuver and / or place the patient in prone position. This strategy could be particularly useful in the context of a major health emergency in centers with limited resources.
Description: Lung aeration measured by ultrasound reaeration score, ranges from 0 (all regions are well aerated) to 36 (all regions are consolidated).
Measure: Effects of a postural recruitment maneuver in lung aeration Time: Through study completion (up to 24 hours)Description: Distribution of ventilation measured by EIT (distribution and changes in the impedance in AU, arbitray units)
Measure: Effects of a postural recruitment maneuver in distribution of ventilation Time: Through study completion (up to 24 hours)Description: Gas exchange measured by blood gas analysis (PaO2, PaCO2, in mmHg) and capnography (end-tidal CO2, in mmHg)
Measure: Effects of a postural recruitment maneuver in gas exchange Time: Through study completion (up to 24 hours)Description: Respiratory mechanics measured by esophageal balloon (esophageal pressure, transpulmonary pressure, in cmH2O)
Measure: Effects of a postural recruitment maneuver in respiratory mechanics Time: Through study completion (up to 24 hours)Description: Hemodynamic data measured by invasive arterial monitoring (mean arterial pressure, in mmHg)
Measure: Effects of a postural recruitment maneuver in hemodynamic Time: Through study completion (up to 24 hours)Description: Oxigenatory tolerance evaluated with pulse oximeter (arterial oxygen saturation, in percentage)
Measure: Feasibility of a postural recruitment maneuver Time: Through study completion (up to 24 hours)Alphabetical listing of all HPO terms. Navigate: Correlations Clinical Trials
Data processed on September 26, 2020.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.
Drug Reports MeSH Reports HPO Reports