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UnknownNCT00479102

Prevention of Iron Deficiency in 2nd Year of Life

Effectiveness of Iron Supplementation in the Second Year of Life for Prevention of Iron Deficiency

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
Sponsor
Soroka University Medical Center · Academic / Other
Sex
All
Age
8 Months – 18 Months
Healthy volunteers
Accepted

Summary

Healthy babies(age 8-18 months) following a routine blood count, with no anemia or iron deficiency, will be randomly placed in two groups. Group 1 will receive a 3 months preventive dose of an iron preparation (Ferripel 3 iron polysaccharide complex). Group 2 will be followed up as a control group. Following a nutritional questionnair, parents of all babies will receive instruction regarding appropriate nutrition in the 2nd year of life. A follow-up blood count will be taken from all participating babies 3 months after recruitment. The study aims to evaluate effectiveness of iron supplementation in the 2nd year of life. The hypothesis is that babies who receive iron supplementation in the 2nd year of life are less likely to develop iron deficiency or anemia.

Conditions

Interventions

TypeNameDescription
DRUGFerripel-3 - iron polysaccharide complex for prevention

Timeline

Start date
2007-05-01
First posted
2007-05-25
Last updated
2007-05-25

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00479102. Inclusion in this directory is not an endorsement.