Name (Synonyms) | Correlation | |
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drug1767 | MinnRAP Peer Support Program Wiki | 1.00 |
Name (Synonyms) | Correlation | |
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D015775 | Fractures, Stress NIH | 1.00 |
D000068376 | Compassion Fatigue NIH | 0.71 |
D000067073 | Psychological Trauma NIH | 0.58 |
D013315 | Stress, Psychological NIH | 0.20 |
D040921 | Stress Disorders, Traumatic NIH | 0.19 |
D013313 | Stress Disorders, Post-Traumatic NIH | 0.18 |
D004194 | Disease NIH | 0.17 |
D001008 | Anxiety Disorders NIH | 0.15 |
Name (Synonyms) | Correlation |
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There is one clinical trial.
The purpose of this proof of concept study is to provide COVID-19 convalescent plasma to patients with moderate to severe COVID-19 and assess: - the titer of anti-COVID-19 antibodies in the donors and in the patients before and after treatment; - the in-depth analysis of immunological parameters in the donors and in recipient before and after treatment; - the impact of plasma transfusion on the reduction of viral load and inflammation - safety and tolerability - clinical efficacy
Description: Semiquantitative measure of viral load by rtPCR for SARS-CoV-2 by nasopharyngeal swabs, at diagnosis and on day 1,3,7
Measure: Viral load decay in the recipient after plasma transfusion with semiquantitative assessment of nasopharyngeal swabs Time: Change from day of diagnosis at day 1Description: 7-point ordinal scale measure on day 0 (Baseline), day 1, 3 and 7 after plasma transfusion
Measure: Number of patients with improvement in the 7-points Ordinal Scale Time: At day 7Description: AE will be assessed by the DAIDS scale on day 1, 3, 7 and 21. Relatedness with plasma transfusion will also be reported.
Measure: Proportion of patients with adverse events, severity of adverse events Time: At day 21