COVID-19 infection. Pneumonia due to SARS-associated coronavirus
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: In the intervention group, patients receive 200 ml of convalescent plasma for one turn Improved plasma for one turn in addition to the standard
Sponsors
Birjand University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Willingness to participate in the studyPeople over the age of 18People with severe form of COVID-19 disease (shortness of breath, respiratory frequency = 30 / min,, blood oxygen saturation = 93%,, partial pressure of arterial oxygen to fraction of inspired oxygen ratio <300,, percentage of pulmonary involvement more than 50 in 24-48 hours,)
Exclusion criteria
Exclusion criteria: -
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body temperature. Timepoint: On days two, three and 7 after hospitalization and receiving plasma. Method of measurement: Thermometer device.;Blood Saturated Oxygen Levels. Timepoint: On days two, three and 7 after hospitalization and receiving plasma. Method of measurement: Pulse oximeter.;C-reactive protein (CRP) Factor. Timepoint: On days two, three and 7 after hospitalization and receiving plasma. Method of measurement: Blood Test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of hospitalization of the patient. Timepoint: End of hospitalization or death of the patient. Method of measurement: By day.;Heart rate. Timepoint: On days two, three and 7 after hospitalization and receiving plasma (patient receives plasma treatment on the second day of hospitalization. Method of measurement: Monitoring device.;Lung lesions on CT scan. Timepoint: On days two, three and 7 after hospitalization and receiving plasma (patient receives plasma treatment on the second day of hospitalization). Method of measurement: Lung lesions with lung CT scan.;D-dimer Factor. Timepoint: On days two, three and 7 after hospitalization and receiving plasma (patient receives plasma treatment on the second day of hospitalization. Method of measurement: blood test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmasood ziaee
Birjand University of Medical Sciences
Outcome results
None listed