| Name (Synonyms) | Correlation | |
|---|---|---|
| drug926 | artus Influenza A/B RT-PCR Test Wiki | 1.00 |
| Name (Synonyms) | Correlation | |
|---|---|---|
| D003384 | Coxsackievirus Infections NIH | 1.00 |
| D000257 | Adenoviridae Infections NIH | 0.71 |
| D018184 | Paramyxoviridae Infections NIH | 0.58 |
| D018357 | Respiratory Syncytial Virus Infections NIH | 0.50 |
| D007251 | Influenza, Human NIH | 0.38 |
| D003141 | Communicable Diseases NIH | 0.12 |
| D014777 | Virus Diseases NIH | 0.11 |
| D007239 | Infection NIH | 0.08 |
| D018352 | Coronavirus Infections NIH | 0.06 |
| Name (Synonyms) | Correlation |
|---|
There is one clinical trial.
I. Study Design: This is a single-arm feasibility study to assess the safety and efficacy of anti-SARS-CoV-2 convalescent plasma (CP) in 1. intubated, mechanically ventilated patients with confirmed COVID-19 pneumonia by chest X-ray or chest CT. 2. hospitalized patients with acute respiratory symptoms between 3 and 7 days after the onset of symptoms, with COVID-19. II. Study Population: 1. Population 1: Mechanically ventilated intubated COVID-19 patients aged 18 years or older. 2. Population 2: Hospitalized COVID-19 patients aged ≥18 years of age with respiratory symptoms within 3 to 7 days from the beginning of illness. III. Study Agent: SARS-CoV-2 convalescent plasma (1-2 units; ~200-400 mL at neutralization antibody titer >1:160.