Developed by Shray Alag, The Harker School
Sections: Correlations,
Clinical Trials, and HPO
Navigate: Clinical Trials and HPO
Name (Synonyms) | Correlation | |
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drug3344 | Respiratory Mechanics Wiki | 1.00 |
drug1482 | FAVIRA 200 MG Film Tablet Wiki | 1.00 |
drug154 | AVIGAN 200 MG Film Tablets Wiki | 1.00 |
Name (Synonyms) | Correlation | |
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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 |
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Navigate: Correlations HPO
There is one clinical trial.
This is a multicenter randomized controlled clinical trial with an 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). The CAVIARDS study is also a basket trial; a basket trial design examines a single intervention in multiple disease populations. CAVIARDS consists of an identical 2-arm mechanical ventilation protocol implemented in two different study populations (COVID-19 and non-COVID-19 patients). As per a typical basket trial design, the operational structure of both the COVID-19 substudy (CAVIARDS-19) and non-COVID-19 substudy (CAVIARDS-all) is shared (recruitment, procedures, data collection, analysis, management, etc.).
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: Duration of ventilation in days
Measure: Duration of ventilation Time: May exceed 60 daysDescription: Duration of ICU and hospital stay in days
Measure: Duration of ICU and hospital stay Time: May exceed 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: Mortality
Measure: Mortality at ICU discharge, 28 days, and hospital discharge Time: Up to date of ICU discharge, 28 days, and hospital dischargeDescription: 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 hoursAlphabetical 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