COVID-19. U07.1 COVID posetive
Conditions
Interventions
Intervention 1: In this study, randomly placed in a group of patients with desferal supplementation at a dose of 20 to 60 mg by weight over 8 to 12 hours, along with 100 mg of vitamin C ampoules at th
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Get infected with a viral infection COVID-19 High serum ferritin levels Increased inflammatory factor in the blood
Exclusion criteria
Exclusion criteria: Patients with renal insufficiency Consumption of desferal supplementary in them is contraindicated
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CRP rate. Timepoint: Before the start of the intervention and the third day after the intervention. Method of measurement: Based on serum surface measurement.;CRP rate. Timepoint: Before the start of the intervention and the third day after the intervention. Method of measurement: Based on serum surface measurement. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFaranak Behnaz
Shahid Beheshti University of Medical Sciences
Outcome results
None listed