Application of Desferal to Treat COVID-19
- 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
Clinical diagnosis of COVID-19 Disease,
Previous history of allergy to Deferoxamin, Pregnancy, kidney dysfunction,
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental: standard treatment Deferoxamine - Experimental: Desferal addition to standard treatment Deferoxamine -
- Primary Outcome Measures
Name Time Method Mortality rate up to 20 days All cause of death
- Secondary Outcome Measures
Name Time Method change in patients clinical manifestation up to 20 days Mild, Moderate or Severe
change in patients PaO2 up to 20 days Length of hospitalization up to 20 days days
C-reactive protein up to 20 days lymphocyte count up to 20 days length of intensive care unit stay 1 to 20 days
Trial Locations
- Locations (1)
Regenerative Medicine Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran
🇮🇷Kermanshah, Iran, Islamic Republic of