NCT00436202

Brief Summary

The purpose of the study is to determine whether improvement in the accessibility to iron supplement will decrease anemia rates in infants.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 15, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 16, 2007

Completed
Last Updated

September 14, 2010

Status Verified

September 1, 2010

First QC Date

February 15, 2007

Last Update Submit

September 12, 2010

Conditions

Keywords

AnemiaIronSupplement

Interventions

Iron supplementBEHAVIORAL

Eligibility Criteria

Age4 Months+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Infant who visit Family Health Centers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tel Aviv District of the Health Office

Tel Aviv, Israel

Location

MeSH Terms

Conditions

Anemia

Interventions

Iron-Dextran Complex

Condition Hierarchy (Ancestors)

Hematologic DiseasesHemic and Lymphatic Diseases

Intervention Hierarchy (Ancestors)

Coordination ComplexesOrganic ChemicalsDextransGlucansPolysaccharidesCarbohydrates

Study Officials

  • Tamar Shohat, M.D., MPH

    Tel Aviv District of the Health Office

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

February 15, 2007

First Posted

February 16, 2007

Last Updated

September 14, 2010

Record last verified: 2010-09

Locations