Skip to content

Iron Supplementation to Reduce Preschoolers Anemia: Comparison Between Intermittent and Cyclic Procedure

Iron Supplementation to Reduce Preschoolers Anemia: Comparison Between Intermittent and Cyclic Procedure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00992823
Enrollment
99
Registered
2009-10-09
Start date
2006-03-31
Completion date
2008-07-31
Last updated
2009-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia

Keywords

Iron, anemia, supplementation, preschoolers, prevalence, preschoolers children from public day care centers

Brief summary

Aim: To evaluate the efficacy of iron supplements given at intervals corresponding to the mean life of red blood cells compared to weekly supplementation, in reducing the prevalence of preschool anemia. Method: Ninety-nine children from public day care centers with ages from 24 to 59 months old were randomly divided into two groups. All the children received 40 doses of 30 mg of ferrous sulfate during a 10-month intervention period. Group 1 received once weekly supplementation and Group 2 received supplementation in two 5-month cycles, each cycle consisting of one month of supplementation (20 workdays) and four months without supplementation.

Detailed description

The prevalence of anemia after the supplementation regimens reduced from 20.20% to 5.05% (P \< 0.0005); the reduction was not significantly different between the two groups (P = 0.35). The mean hemoglobin concentration increased in both groups (Group 1: 0.27 g/dL; P \< 0.016 and Group 2: 0.47 g/dL; P \< 0.0005) without significant differences between the groups (P = 0.17).

Interventions

40 doses of 30 mg of ferrous sulfate during a 10-month intervention period

Sponsors

Sao Jose do Rio Preto Medical School
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
24 Months to 59 Months
Healthy volunteers
Yes

Inclusion criteria

* The participants of the study were children with ages ranging from 24 to 59 months old that attended four local public day care centers

Exclusion criteria

* Presence of infection or reported infections within two weeks prior to the intervention * Anemia lower than 7.0 g/dL and children taking medications containing ferrous sulfate

Design outcomes

Primary

MeasureTime frame
Initial and final blood hemoglobin concentration10 months

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026