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Study aim
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Evaluation of the effects of Desferal on clinical symptoms in patients with COVID-19
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Design
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A phase 2-3 clinical trial with parallel group, open-label, 60 patients, block randomized method
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Settings and conduct
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This study will be conducted at the Shahid Mohammadi Hospital, Hormozgan University of Medical Sciences, Bandar Abbas.The study population is 60 patients with COVID-19 (30 patients in control group, and 30 in study group).
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Participants/Inclusion and exclusion criteria
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Inclusion criteria: Age >18 years, positive polymerase chain reaction (PCR) test for COVID-19, primary clinical symptoms, hospitalized and moderate patients, and signing informed consent.
criteria: Underlying diseases, including renal failure (serum creatinine >2), myocarditis and arrhythmia, anemia (hemoglobin<4-8), lower respiratory tract infection, and asthma, patients requiring intubation or frequent use of respiratory drugs, severe and critical patients, history of allergy to studied drug, and pregnancy and breastfeeding
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Intervention groups
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Group A will be patients receiving standard treatment of COVID-19 according to the Ministry of Health's protocol. Group B will be patients receiving, in addition to the standard treatment, Deferoxamine solution (500 mg) divided in four doses a day through a nebulizer for 7 days.
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Main outcome variables
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Checking the viral load, fever, O2 saturation, Evaluation of duration of hospitalization, C-reactive protein, Occurrence of adverse drug reactions