Name (Synonyms) | Correlation | |
---|---|---|
drug3137 | XCEL-UMC-BETA Wiki | 0.58 |
drug1439 | Interferon-Beta Wiki | 0.58 |
drug240 | Apixaban 2.5 MG Wiki | 0.58 |
drug1840 | Nasopharyngeal and throat/oropharyngeal swabs analyses by RT-PCR and ddPCR Wiki | 0.58 |
drug241 | Apixaban 5MG Wiki | 0.58 |
drug2633 | Simvastatin Wiki | 0.41 |
drug2458 | Rivaroxaban Wiki | 0.26 |
drug1607 | Losartan Wiki | 0.20 |
drug703 | Colchicine Wiki | 0.18 |
drug2122 | Placebo Wiki | 0.06 |
Name (Synonyms) | Correlation | |
---|---|---|
D013927 | Thrombosis NIH | 0.13 |
D013577 | Syndrome NIH | 0.06 |
D055371 | Acute Lung Injury NIH | 0.06 |
D012127 | Respiratory Distress Syndrome, Newborn NIH | 0.05 |
D012128 | Respiratory Distress Syndrome, Adult NIH | 0.05 |
D045169 | Severe Acute Respiratory Syndrome NIH | 0.03 |
D018352 | Coronavirus Infections NIH | 0.02 |
Name (Synonyms) | Correlation |
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There are 3 clinical trials
ACT is a randomized clinical trial to assess therapies to reduce the clinical progression of COVID-19.
Description: composite of hospitalization or death
Measure: Outpatient trial - Colchicine vs. control and Aspirin vs. control Time: 45 days post randomizationDescription: invasive mechanical ventilation or death
Measure: Inpatient trial - Interferon-β vs. control and Colchicine vs. control Time: 45 days post randomizationDescription: invasive mechanical ventilation or death
Measure: Inpatient trial - Aspirin and rivaroxaban vs. control Time: 45 days post randomizationDescription: disease progression by 2 points on a 7-point scale
Measure: Outpatient and Inpatient trials - Colchicine vs. control, Interferon-β vs. control Time: 45 days post randomizationDescription: composite of major adverse cardiovascular events (MI, stroke, ALI, VTE, death), and disease progression by 2 points on a 7-point scale
Measure: Outpatient and Inpatient trials - Aspirin vs. control, Aspirin and rivaroxaban vs. control Time: 45 days post randomizationThe CRASH-19 trial is a multinational, open-label, factorial, randomised trial in adults hospitalised with suspected or confirmed acute COVID-19 infection.
Description: Cause of death will be described
Measure: Death Time: up to 28 days of randomisationA multi-center adaptive randomized placebo-controlled platform trial evaluating the efficacy and safety of anti-thrombotic strategies in COVID-19 adults not requiring hospitalization at time of diagnosis
Description: The primary outcome will be a composite endpoint of need for hospitalization for cardiovascular/pulmonary events, symptomatic deep venous thrombosis, pulmonary embolism, arterial thromboembolism, myocardial infarction, ischemic stroke, and all-cause mortality for up to 45 days after initiation of assigned treatment.
Measure: Primary Time: 45 days