Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
260 participants
OBSERVATIONAL
2010-02-28
2014-08-31
Brief Summary
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Detailed Description
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Two groups of children will be included, 200 children from Jewish origin and 200 from non Jewish origin, mostly Arabs.
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient.
The laboratory analysis will include complete blood count and serum ferritin analysis.
Children that were previously diagnosed suffering from iron deficiency, children suffering from chronic diseases or were born premature will not be included in the study.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Toddlers from Jewish origin
Toddlers from Jewish origin aged 18 to 36 months
Questionnaire filling and laboratory analysis
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient.
The laboratory analysis will include complete blood count and serum ferritin analysis.
Toddlers from non Jewish origin
Toddlers aged 18 to 36 months belonging to non Jewish (Arab) population
Questionnaire filling and laboratory analysis
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient.
The laboratory analysis will include complete blood count and serum ferritin analysis.
Interventions
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Questionnaire filling and laboratory analysis
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient.
The laboratory analysis will include complete blood count and serum ferritin analysis.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Children suffering from chronic diseases or were born premature will not be included in the study.
18 Months
36 Months
ALL
Yes
Sponsors
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HaEmek Medical Center, Israel
OTHER
Responsible Party
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Dr Koren Ariel
Head of Pediatric Hematology Unit and Pediatric Dpt B
Principal Investigators
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Ariel Koren, MD
Role: PRINCIPAL_INVESTIGATOR
Pediatric Dpt B and Pediatric Hemaology Unit - Ha'Emek Medical Center - Afula - Israel
Locations
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Pediatric Hematology Unit - Ha'Emek Medical Center
Afula, Afula, Israel
Countries
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Other Identifiers
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0024/09-EMC
Identifier Type: -
Identifier Source: org_study_id
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