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The Effect of Early Iron Deficiency on Developmental Brain and Behavior in Infants

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00515918
Acronym
IDBB
Enrollment
Unknown
Registered
2007-08-14
Start date
2007-09-30
Completion date
2010-09-30
Last updated
2007-08-14

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

Conditions

Iron Deficiency

Keywords

Iron deficiency, brain, cognition, behavior

Brief summary

The purpose of this project to examine brain functions and behavior related to ID including sensory ,motor, cognitive and social /emotional functioning, and address unanswered questions about brain and behavior impacts of different timing of ID(pre- and /or postnatal ID) in infants.

Detailed description

Iron deficiency (ID) is the most common single nutrient disorder in the world. Pregnant women and children before pre-school age are at highest risk. Data from animal models provide evidence that early ID affected developing brain in specific regions and functions by varies processes include myelination, dopamine neurotransmitter system, and neurometabolism. These impacts appeared differential at different time of brain development and different brain regions, depending on the timing of ID. The reversibility of these effects also appeared to depend on the timing of ID. This project uses innovative neuropsychologic/ neurophysiologic and behavioral techniques, such as event-related potentials(ERP), ABR and VEP, to study brain functions and behavior related to ID including sensory ,motor, cognitive and social /emotional functioning, and address unanswered questions about brain and behavior impacts of different timing of ID(pre- and /or postnatal ID) in the human infants. This research has the potential to understand reversibility of effects depending on timing of ID and treatment as well as basic understanding of mechanism of impact of ID in human developing brain. It may also have important implications with regard to policy of interventions for different timing of ID, and improve children early development and the quality of population.

Interventions

DIETARY_SUPPLEMENTiron

Sponsors

Zhejiang University
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 36 Months

Inclusion criteria

* Full- term infants

Exclusion criteria

* Prematures, * Perinatal high risk infants(asphyxia,infection etc.), * Maternal alcohol, * Smoking, * Drug abuse, * Inherited diseases

Countries

China

Contacts

Primary ContactJie Shao, M.D
shaojie@zju.edu.cn+86-571-87061007

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026