None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. You must have the consent of informed consent. 2. Have an age between 6 months and 2 years. 3. Hemoglobin> 8 and <11 g / dl. and / or decreased serum Ferritin 4. Be able to attend the consultation according to the study schedule. 5. Be included between the 10-90 percentiles, age-statural for age and sex according to the NCHS tables.
Exclusion criteria
Exclusion criteria: 1. History of intolerance to iron salts. 2. History of chronic anemia resistant to treatment. 3. Acute or chronic pathologies that can modify the blood values. 4. Intestinal parasitosis detected by simple direct examination at the time of onset of the study. 5. Need to use medications that can modify the blood values. 6. History of blood discies. 7. History of liver or kidney pathology.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome name:Ferritin levels Measure:Ferritin levels achieved at twelve weeks in patients of both groups with pharyngeal polymodal Timepoints:12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Outcome name:Percentage of patients who are withdrawn from the study due to adverse reactions. Measure:Percentage of patients who are withdrawn from the study due to adverse reactions. Timepoints:12 weeks | — |
Countries
Peru