Skip to main content
Clinical Trials/NCT00992823
NCT00992823
Completed
Not Applicable

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

Sao Jose do Rio Preto Medical School1 site in 1 country99 target enrollmentMarch 2006

Overview

Phase
Not Applicable
Intervention
iron supplementation
Conditions
Anemia
Sponsor
Sao Jose do Rio Preto Medical School
Enrollment
99
Locations
1
Primary Endpoint
Initial and final blood hemoglobin concentration
Status
Completed
Last Updated
16 years ago

Overview

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).

Registry
clinicaltrials.gov
Start Date
March 2006
End Date
July 2008
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Sao Jose do Rio Preto Medical School

Eligibility Criteria

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

Arms & Interventions

Group 1:iron weekly supplementation

Intervention: iron supplementation

Group 2: cycle supplementation

two 5-month cycles, each cycle consisting of one month of supplementation (20 workdays) and four months without supplementation.

Intervention: iron supplementation

Outcomes

Primary Outcomes

Initial and final blood hemoglobin concentration

Time Frame: 10 months

Study Sites (1)

Loading locations...

Similar Trials