Clinical Trials Directory

Trials / Completed

CompletedNCT02196337

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

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

Status
Completed
Phase
Study type
Observational
Enrollment
8,000 (actual)
Sponsor
Swiss Federal Institute of Technology · Academic / Other
Sex
All
Age
2 Weeks – 44 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2014-07-01
Primary completion
2016-01-01
Completion
2016-01-01
First posted
2014-07-22
Last updated
2016-04-19

Locations

4 sites across 4 countries: China, Croatia, Philippines, Switzerland

Source: ClinicalTrials.gov record NCT02196337. Inclusion in this directory is not an endorsement.