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Evaluation of an Intervention Program for the Prevention of Anemia

NCT00436202 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2010-09-14

No results posted yet for this study

Summary

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

Conditions

Interventions

BEHAVIORAL

Iron supplement

Sponsors & Collaborators

  • Tel Aviv District of the Health Office

    collaborator UNKNOWN

  • Wolfson Medical Center

    lead OTHER_GOV

Principal Investigators

  • Tamar Shohat, M.D., MPH · Tel Aviv District of the Health Office

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
4 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Countries

  • Israel

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00436202 on ClinicalTrials.gov