COVID-19. Coronavirus infection, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Acetaminophen + Febuxostat. Intervention 2: Control group: Acetaminophen + Hydroxychloroquine.
Sponsors
Mazandaran University of Medical Sceinces
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients infected with COVID-19
Exclusion criteria
Exclusion criteria: Severe disease patients that need hospitalization.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CT-scan findings. Timepoint: Before the intervention and 2 weeks after the intervention. Method of measurement: CT-scan. | — |
Secondary
| Measure | Time frame |
|---|---|
| Fever. Timepoint: Before the intervention and 5 days after the intervention. Method of measurement: Thermometer.;Lymphocyte count. Timepoint: Before the intervention and 5 days after the intervention. Method of measurement: CBC test.;CRP. Timepoint: Before the intervention and 5 days after the intervention. Method of measurement: Laboratory. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactLotfollah Davoodi
Mazandaran University of Medical Sciences
Outcome results
None listed