Salt Iodization: Meeting the Needs of Pregnancy, Lactation and Infancy — SIMPLIFY  

Iodine Deficiency Clinical Trial

Official title: Salt Iodization and the 1st 1000 Days: Does a USI Program Cover the Iodine Requirement of Pregnant and Lactating Women and Infants?

Status Completed

Clinical Trial Summary

The purpose of this study is to determine whether universal salt iodization (USI) meets the iodine requirements of pregnant women, lactating women and infants.

Clinical Trial Description

Because pregnant women, lactating women and infants are the groups most vulnerable to iodine deficiency and its irreversible consequences, programs should focus on these groups. But like other mass fortification strategies, it is uncertain whether USI can meet the increased dietary requirements of pregnant women, lactating women and infants. Objective of this study to test whether USI can meet the dietary requirements of iodine in women of reproductive age, pregnant women, lactating women and infants up to 2 years of age without causing excess iodine intake in school children and non-pregnant non-lactating women. The study hypothesis is that USI, when fortified at adequate levels and applied to all salt consumed, including both household salt and salt used for processed foods, provides adequate dietary iodine for all population groups, except for weaning infants; while not posing any risk of excessive iodine intakes in other age groups. ;

Study Design

Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Iodine Deficiency

• NCT number: NCT02196337
• Study type: Observational
• Source: Swiss Federal Institute of Technology
• Status: Completed
• Phase: N/A
• Start date: July 2014
• Completion date: January 2016