Viewing Study NCT00436202



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Last Modification Date: 2024-10-26 @ 9:30 AM
Study NCT ID: NCT00436202
Status: UNKNOWN
Last Update Posted: 2010-09-14
First Post: 2007-02-15

Brief Title: Evaluation of an Intervention Program for the Prevention of Anemia
Sponsor: Wolfson Medical Center
Organization: Wolfson Medical Center

Study Overview

Official Title: None
Status: UNKNOWN
Status Verified Date: 2010-09
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of the study is to determine whether improvement in the accessibility to iron supplement will decrease anemia rates in infants
Detailed Description: Iron deficiency anemia is the most common type of anemia in infants children and women of reproductive age The most frequent cause of iron deficiency in infants at 6 months of life is poor nutrition during a period of rapid growth and a diet lacking in iron rich foods Children who suffered from anemia in infancy demonstrated slower cognitive development were low achievers in school and had a high rate of behavioral disturbances

The Ministry of Health implements a primary prevention program for anemia If by making iron supplements more accessible would increase parental compliance in acquisition of the iron supplement and subsequently reduce the rate of iron deficiency anemia the result would be the immediate application of the finding It is possible to implement a program whereby the supplement will be directly available at the family health centers for purchase by the parent

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None