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Application of Desferal to Treat COVID-19

Phase 1
Conditions
COVID-19
Interventions
Registration Number
NCT04333550
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
Inclusion Criteria

Clinical diagnosis of COVID-19 Disease,

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Exclusion Criteria

Previous history of allergy to Deferoxamin, Pregnancy, kidney dysfunction,

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental: standard treatmentDeferoxamine-
Experimental: Desferal addition to standard treatmentDeferoxamine-
Primary Outcome Measures
NameTimeMethod
Mortality rateup to 20 days

All cause of death

Secondary Outcome Measures
NameTimeMethod
change in patients clinical manifestationup to 20 days

Mild, Moderate or Severe

change in patients PaO2up to 20 days
Length of hospitalizationup to 20 days

days

C-reactive proteinup to 20 days
lymphocyte countup to 20 days
length of intensive care unit stay1 to 20 days

Trial Locations

Locations (1)

Regenerative Medicine Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran

🇮🇷

Kermanshah, Iran, Islamic Republic of

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