PACTR202404915122192
Completed
Phase 4
A comparative study to evaluate the efficacy and tolerability of new generations of iron preparations with traditional iron therapy in pediatrics: A prospective randomized controlled trial.
Menoufia faculty of medicine0 sites87 target enrollmentFebruary 19, 2024
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Haematological Disorders
- Sponsor
- Menoufia faculty of medicine
- Enrollment
- 87
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age range 6 months till 59 months old
- •no evidence of infection and negative c–reactive protein (CRP)
- •hemoglobin below the WHO stipulated cutoff values to define IDA anemia: hemoglobin \<11\.0 g/dL, MCV \<73 fL and serum ferritin \< 12 mg/L.
- •no history of consumption of iron supplements for 4 months ago or history of blood transfusion.
Exclusion Criteria
- •Children who had any signs of infection (fever, vomiting or diarrhea) on blood collection days,
- •children with anemia rather than IDA e.g. hemolytic anemia or haemoglobinopathy (sickle cell disease, beta thalassemia major)
- •children with chronic diseases or drugs that may affect iron absorption
Outcomes
Primary Outcomes
Not specified
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