Name (Synonyms) | Correlation | |
---|---|---|
drug1634 | Non-convalescent fresh frozen plasma (Standard plasma) Wiki | 1.00 |
Name (Synonyms) | Correlation | |
---|---|---|
D025241 | Spondylarthritis NIH | 1.00 |
D001167 | Arteritis NIH | 0.71 |
D012859 | Sjogren's Syndrome NIH | 0.71 |
D001327 | Autoimmune Diseases NIH | 0.58 |
D011111 | Polymyalgia Rheumatica NIH | 0.58 |
D013700 | Giant Cell Arteritis NIH | 0.58 |
D008180 | Lupus Erythematosus, Systemic NIH | 0.41 |
D001172 | Arthritis, Rheumatoid NIH | 0.38 |
D001168 | Arthritis NIH | 0.29 |
Name (Synonyms) | Correlation | |
---|---|---|
HP:0012089 | Arteritis HPO | 0.71 |
HP:0002960 | Autoimmunity HPO | 0.58 |
HP:0002725 | Systemic lupus erythematosus HPO | 0.41 |
HP:0001370 | Rheumatoid arthritis HPO | 0.38 |
HP:0001369 | Arthritis HPO | 0.29 |
There is one clinical trial.
The clinical trial aims to study the safety and efficacy of transfusion of COVID-19 convalescent hyperimmune plasma for the treatment of moderate and severe forms of COVID-19 disease in comparison with non-convalescent fresh frozen plasma (standard plasma).
Description: The number and proportion of patients with the normal body temperature (≤37.2 C) at the days 1, 2, 3, 4, 5, 6, 7 after the start of therapy, for the statistical data comparison between the two arms.
Measure: The number and proportion of patients with the normal body temperature (≤37.2 C) at the day 1, 2, 3, 4, 5, 6, 7 after the start of therapy Time: Days 1, 2, 3, 4, 5, 6, 7Description: For each patient, the number of days passed from the plasma administration to placing on mechanical ventilation will be noted, for the statistical data comparison between the two arms.
Measure: Days before mechanical ventilation Time: 30 daysDescription: For each patient, the number of days he or she spent on the oxygen support after the plasma administration will be noted, for the statistical data comparison between the two arms.
Measure: Days of need for oxygen therapy Time: 30 daysDescription: For each patient, the entire duration of ICU stay after the plasma administration will be noted, for the statistical data comparison between the two arms.
Measure: Days of stay in the ICU Time: 30 daysDescription: For each patient, the entire duration of hospital stay after the plasma administration will be noted, for the statistical data comparison between the two arms.
Measure: Days of hospitalization Time: 30 daysDescription: Changes of the plasma levels of the SARS-CoV-2 antibodies, days 14 and 30 after the treatment start vs those levels before the treatment start (day 0) for the same patients.
Measure: Changes of the titer of the SARS-CoV-2 antibodies in the blood plasma of patients Time: Days 0, 14, 30Description: Changes of the plasma levels of IL2, IL6, IL10, TNFalpha and INFgamma, days 3 and 7 after the treatment start vs those levels before the treatment start (day 0) for the same patients.
Measure: Dynamics of the cytokine profile Time: Days 0, 3, 7Description: Incidence of administering IL6 receptor blockers (tocilizumab, sarilumab)
Measure: Incidence of the cytokine storm development and the need of administering cytokine storm inhibitors Time: Days 3, 7Description: Changes of the plasma levels of C-reactive protein, days 1, 2, 3, 4, 5, 6, 7 after the treatment start vs those levels before the treatment start (Day 0) for the same patients.
Measure: Dynamics of the level of C-reactive protein Time: Days 0, 1, 2, 3, 4, 5, 6, 7Description: 30-day mortality rate, for the statistical data comparison between the two arms.
Measure: 30-day mortality rate Time: 30 days