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In this study, defined cases of COVID-19 with mild, moderate or severe pneumonia will be treated with standard treatment regimens in combination with IV injection of Deferoxamine. Improvement in clinical, laboratory and radiological manifestations will be evaluated in treated patient compared to control group.
Enrollment
Sex
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Volunteers
Inclusion criteria
Clinical diagnosis of COVID-19 Disease,
Exclusion criteria
Previous history of allergy to Deferoxamin, Pregnancy, kidney dysfunction,
Primary purpose
Allocation
Interventional model
Masking
50 participants in 2 patient groups
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Central trial contact
Alireza Ghaffarieh, MD; Yadollah Shakiba, MD, PhD
Data sourced from clinicaltrials.gov
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