Clinical Trials Directory

Trials / Completed

CompletedNCT00992823

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
99 (actual)
Sponsor
Sao Jose do Rio Preto Medical School · Academic / Other
Sex
All
Age
24 Months – 59 Months
Healthy volunteers
Accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGiron supplementation40 doses of 30 mg of ferrous sulfate during a 10-month intervention period
BIOLOGICALiron supplementationsupplementation in two 5-month cycles, each cycle consisting of one month of supplementation (20 workdays) and four months without supplementation.

Timeline

Start date
2006-03-01
Primary completion
2007-02-01
Completion
2008-07-01
First posted
2009-10-09
Last updated
2009-10-15

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00992823. Inclusion in this directory is not an endorsement.