|drug2052||Mindfulness + Compassion Intervention (MC) Wiki||0.71|
|drug2053||Mindfulness Alone (MO) Intervention Wiki||0.71|
|D018352||Coronavirus Infections NIH||0.03|
There are 2 clinical trials
This study will evaluate the efficacy, safety, pharmacodynamics, and pharmacokinetics of tocilizumab (TCZ) compared with a matching placebo in combination with standard of care (SOC) in hospitalized patients with severe COVID-19 pneumonia.
The mortality rate of the disease caused by the corona virus induced disease (COVID-19) has been estimated to be 3.7% (WHO), which is more than 10-fold higher than the mortality of influenza. Patients with certain risk factors seem to die by an overwhelming reaction of the immune system to the virus, causing a cytokine storm with features of Cytokine-Release Syndrome (CRS) and Macrophage Activation Syndrome (MAS) and resulting in Acute Respiratory Distress Syndrome (ARDS). Several pro-inflammatory cytokines are elevated in the plasma of patients and features of MAS in COVID-19, include elevated levels of ferritin, d-dimer, and low platelets. There is increasing data that cytokine-targeted biological therapies can improve outcomes in CRS or MAS and even in sepsis. Tocilizumab (TCZ), an anti-IL-6R biological therapy, has been approved for the treatment of CRS and is used in patients with MAS. Based on these data, it is hypothesized that TCZ can reduce mortality in patients with severe COVID-19 prone to CRS and ARDS. The overall purpose of this study is to evaluate whether treatment with TCZ reduces the severity and mortality in patients with COVID-19.
Description: Assessed by the 8-point WHO scaleMeasure: Illness severity Time: At days 2, 7, 14, 28 after randomisation
Description: Clinical improvement is defined as a ≥ 2-point improvement in the 8-point WHO scaleMeasure: Number of patients with clinical improvement Time: At days 2, 7, 14, 28 after randomisation
Description: Clinical improvement is defined as a ≥ 2-point improvement in the 8-point WHO scaleMeasure: Time to clinical improvement (days) Time: Up to day 28 after randomisation
Description: Events of special interest are defined as secondary infections, acute kidney failure, hepatic, and cardiac failureMeasure: Number of patients with events of special interest Time: Within 28 days after randomisation
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